Canonical Allele Identifier: CA385181765

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56087064G>C (hg19) ; chr12:g.55693280G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693280G>C , CM000674.2:g.55693280G>C	GRCh38
NC_000012.11:g.56087064G>C , CM000674.1:g.56087064G>C	GRCh37
NC_000012.10:g.54373331G>C	NCBI36
NG_012343.1:g.24026C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2197C>G	ENSP00000452467.1:n.*2197C>G
ENST00000554327.6:c.1244C>G
ENST00000557058.2:n.1988C>G
ENST00000557257.2:c.2099C>G	ENSP00000450578.2:p.Ser700Cys
ENST00000557555.3:c.2585C>G	ENSP00000451039.3:p.Ser862Cys
ENST00000686981.1:c.*2284C>G	ENSP00000510795.1:n.*2284C>G
ENST00000687390.1:n.679C>G
ENST00000691052.1:c.*1057C>G	ENSP00000508886.1:n.*1057C>G
ENST00000691846.1:c.1386C>G
ENST00000691973.1:c.2585C>G	ENSP00000509141.1:p.Ser862Cys
ENST00000257879.11:c.2573C>G MANE Select	ENSP00000257879.7:p.Ser858Cys
ENST00000553804.6:c.2585C>G	ENSP00000452120.1:p.Ser862Cys
ENST00000257879.10:c.2573C>G	ENSP00000257879.6:p.Ser858Cys
ENST00000347027.10:c.2555C>G	ENSP00000343009.6:p.Ser852Cys
ENST00000452168.6:c.2294C>G	ENSP00000393844.2:p.Ser765Cys
ENST00000553804.5:c.2585C>G	ENSP00000452120.1:p.Ser862Cys
ENST00000554327.5:c.638C>G
ENST00000555728.5:c.2705C>G	ENSP00000452387.1:p.Ser902Cys
NM_001144996.1:c.2585C>G	NP_001138468.1:p.Ser862Cys
NM_001144997.1:c.2294C>G	NP_001138469.1:p.Ser765Cys
NM_002206.2:c.2573C>G	NP_002197.2:p.Ser858Cys
XM_005268839.1:c.2705C>G	XP_005268896.1:p.Ser902Cys
XM_005268840.1:c.2687C>G	XP_005268897.1:p.Ser896Cys
XM_005268841.1:c.2705C>G	XP_005268898.1:p.Ser902Cys
XM_005268842.1:c.2555C>G	XP_005268899.1:p.Ser852Cys
XM_005268844.1:c.2366C>G	XP_005268901.1:p.Ser789Cys
XM_005268845.1:c.2234C>G	XP_005268902.1:p.Ser745Cys
XM_005268846.1:c.2234C>G	XP_005268903.1:p.Ser745Cys
XM_005268847.1:c.2231C>G	XP_005268904.1:p.Ser744Cys
XM_005268848.1:c.2231C>G	XP_005268905.1:p.Ser744Cys
XM_005268849.1:c.2231C>G	XP_005268906.1:p.Ser744Cys
XM_005268850.1:c.2099C>G	XP_005268907.1:p.Ser700Cys
XM_011538286.1:c.2366C>G	XP_011536588.1:p.Ser789Cys
XM_005268839.2:c.2705C>G	XP_005268896.1:p.Ser902Cys
XM_005268840.2:c.2687C>G	XP_005268897.1:p.Ser896Cys
XM_005268841.2:c.2705C>G	XP_005268898.1:p.Ser902Cys
XM_005268842.2:c.2555C>G	XP_005268899.1:p.Ser852Cys
XM_017019265.1:c.2315C>G	XP_016874754.1:p.Ser772Cys
NM_001144996.2:c.2585C>G	NP_001138468.1:p.Ser862Cys
NM_001367993.1:c.2246C>G	NP_001354922.1:p.Ser749Cys
NM_001367994.1:c.1229C>G	NP_001354923.1:p.Ser410Cys
NM_001374465.1:c.2555C>G	NP_001361394.1:p.Ser852Cys
NM_002206.3:c.2573C>G MANE Select	NP_002197.2:p.Ser858Cys