Canonical Allele Identifier: CA357925621

Gene: LARP7 MIR302CHG

Linked Data

• MyVariant Identifiers: chr4:g.113568509A>T (hg19) ; chr4:g.112647353A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.112647353A>T , CM000666.2:g.112647353A>T	GRCh38
NC_000004.11:g.113568509A>T , CM000666.1:g.113568509A>T	GRCh37
NC_000004.10:g.113787958A>T	NCBI36
NG_032779.1:g.15390A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505034.6:c.801A>T (LARP7)	ENSP00000421541.2:p.Glu267Asp
ENST00000505216.2:c.*560A>T (LARP7)	ENSP00000424116.1:n.*560A>T
ENST00000694891.1:c.798A>T (LARP7)	ENSP00000511571.1:p.Glu266Asp
ENST00000694894.1:c.801A>T (LARP7)	ENSP00000511572.1:p.Glu267Asp
ENST00000694895.1:c.801A>T (LARP7)	ENSP00000511573.1:p.Glu267Asp
ENST00000694896.1:c.801A>T (LARP7)	ENSP00000511574.1:p.Glu267Asp
ENST00000694897.1:c.*200A>T (LARP7)	ENSP00000511575.1:n.*200A>T
ENST00000694898.1:c.801A>T (LARP7)	ENSP00000511576.1:p.Glu267Asp
ENST00000694899.1:c.798A>T (LARP7)	ENSP00000511577.1:p.Glu266Asp
ENST00000694900.1:c.801A>T (LARP7)	ENSP00000511578.1:p.Glu267Asp
ENST00000694901.1:c.*560A>T (LARP7)	ENSP00000511579.1:n.*560A>T
ENST00000511529.2:c.798A>T (LARP7)	ENSP00000426376.2:p.Glu266Asp
ENST00000512361.2:n.981A>T (LARP7)
ENST00000512589.6:c.*607A>T (LARP7)	ENSP00000426709.1:n.*607A>T
ENST00000684864.1:c.801A>T (LARP7)	ENSP00000509993.1:p.Glu267Asp
ENST00000688617.1:n.1075A>T (LARP7)
ENST00000689262.1:n.1952A>T (LARP7)
ENST00000689844.1:c.801A>T (LARP7)	ENSP00000509899.1:p.Glu267Asp
ENST00000690008.1:c.*560A>T (LARP7)	ENSP00000508938.1:n.*560A>T
ENST00000692075.1:n.1037A>T (LARP7)
ENST00000692168.1:n.967A>T (LARP7)
ENST00000692416.1:c.564A>T (LARP7)	ENSP00000509527.1:p.Glu188Asp
ENST00000693375.1:c.564A>T (LARP7)	ENSP00000508585.1:p.Glu188Asp
ENST00000693442.1:c.801A>T (LARP7)	ENSP00000509975.1:p.Glu267Asp
ENST00000344442.10:c.801A>T (LARP7) MANE Select	ENSP00000344950.5:p.Glu267Asp
ENST00000651579.1:c.801A>T (LARP7)	ENSP00000499190.1:p.Glu267Asp
ENST00000324052.10:c.801A>T (LARP7)	ENSP00000314311.6:p.Glu267Asp
ENST00000344442.9:c.801A>T (LARP7)	ENSP00000344950.5:p.Glu267Asp
ENST00000505034.5:c.801A>T (LARP7)	ENSP00000421541.1:p.Glu267Asp
ENST00000509061.5:c.822A>T (LARP7)	ENSP00000422626.1:p.Glu274Asp
ENST00000509622.5:c.*560A>T (LARP7)	ENSP00000422451.1:n.*560A>T
ENST00000511529.1:c.143A>T (LARP7)
ENST00000513553.5:c.31-366A>T (LARP7)	ENSP00000422013.1:n.31-366A>T
NM_001267039.1:c.822A>T (LARP7)	NP_001253968.1:p.Glu274Asp
NM_015454.2:c.801A>T (LARP7)	NP_056269.1:p.Glu267Asp
NM_016648.3:c.801A>T (LARP7)	NP_057732.2:p.Glu267Asp
NR_049768.1:n.976A>T (LARP7)
NR_146092.1:n.148-385T>A (MIR302CHG)
NR_146093.1:n.103+62T>A (MIR302CHG)
NR_146094.1:n.51-385T>A (MIR302CHG)
XM_024454080.1:c.801A>T (LARP7)	XP_024309848.1:p.Glu267Asp
XM_024454081.1:c.801A>T (LARP7)	XP_024309849.1:p.Glu267Asp
XM_024454082.1:c.801A>T (LARP7)	XP_024309850.1:p.Glu267Asp
XM_024454083.1:c.801A>T (LARP7)	XP_024309851.1:p.Glu267Asp
XM_024454084.1:c.801A>T (LARP7)	XP_024309852.1:p.Glu267Asp
XM_024454085.1:c.801A>T (LARP7)	XP_024309853.1:p.Glu267Asp
XM_024454086.1:c.564A>T (LARP7)	XP_024309854.1:p.Glu188Asp
XM_024454087.1:c.564A>T (LARP7)	XP_024309855.1:p.Glu188Asp
XM_024454088.1:c.564A>T (LARP7)	XP_024309856.1:p.Glu188Asp
XM_024454089.1:c.120A>T (LARP7)	XP_024309857.1:p.Glu40Asp
NM_016648.4:c.801A>T (LARP7) MANE Select	NP_057732.2:p.Glu267Asp
NM_001370974.1:c.801A>T (LARP7)	NP_001357903.1:p.Glu267Asp
NM_001370975.1:c.801A>T (LARP7)	NP_001357904.1:p.Glu267Asp
NM_001370976.1:c.798A>T (LARP7)	NP_001357905.1:p.Glu266Asp
NM_001370977.1:c.798A>T (LARP7)	NP_001357906.1:p.Glu266Asp
NM_001370978.1:c.801A>T (LARP7)	NP_001357907.1:p.Glu267Asp
NM_001370979.1:c.798A>T (LARP7)	NP_001357908.1:p.Glu266Asp
NM_001370980.1:c.798A>T (LARP7)	NP_001357909.1:p.Glu266Asp
NM_001370981.1:c.564A>T (LARP7)	NP_001357910.1:p.Glu188Asp
NM_001370982.1:c.564A>T (LARP7)	NP_001357911.1:p.Glu188Asp
NM_001267039.2:c.822A>T (LARP7)	NP_001253968.1:p.Glu274Asp
NM_015454.3:c.801A>T (LARP7)	NP_056269.1:p.Glu267Asp
NM_001267039.4:c.801A>T (LARP7)	NP_001253968.2:p.Glu267Asp