Canonical Allele Identifier: CA2205180

Gene: RNPEPL1

Linked Data

• dbSNP Id: rs770772897
• ExAC: 2:241516071 C / T
• gnomAD v2: 2-241516071-C-T
• MyVariant Identifiers: chr2:g.241516071C>T (hg19) ; chr2:g.240576654C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576654C>T , CM000664.2:g.240576654C>T	GRCh38
NC_000002.11:g.241516071C>T , CM000664.1:g.241516071C>T	GRCh37
NC_000002.10:g.241164744C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1630C>T MANE Select	ENSP00000270357.4:p.Pro544Ser
ENST00000270357.8:c.937C>T	ENSP00000270357.3:p.Pro313Ser
ENST00000437406.1:c.196C>T	ENSP00000403319.1:p.Pro66Ser
ENST00000451363.5:c.271C>T	ENSP00000414661.1:p.Pro91Ser
ENST00000464550.5:n.466C>T
ENST00000471657.1:n.433C>T
ENST00000481757.5:n.2564C>T
ENST00000486058.5:n.1743C>T
ENST00000493398.5:n.776C>T
NM_018226.4:c.1630C>T	NP_060696.4:p.Pro544Ser
XM_005247036.3:c.1597C>T	XP_005247093.1:p.Pro533Ser
NM_018226.5:c.1630C>T	NP_060696.4:p.Pro544Ser
XM_005247036.4:c.1597C>T	XP_005247093.1:p.Pro533Ser
NM_018226.6:c.1630C>T MANE Select	NP_060696.4:p.Pro544Ser