Canonical Allele Identifier: CA359786169

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177639T>C (hg19) ; chr5:g.56881812T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881812T>C , CM000667.2:g.56881812T>C	GRCh38
NC_000005.9:g.56177639T>C , CM000667.1:g.56177639T>C	GRCh37
NC_000005.8:g.56213396T>C	NCBI36
NG_031884.1:g.71740T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2612T>C MANE Select	ENSP00000382423.3:p.Leu871Ser
ENST00000399503.3:c.2612T>C	ENSP00000382423.3:p.Leu871Ser
NM_005921.1:c.2612T>C	NP_005912.1:p.Leu871Ser
XM_005248519.3:c.2234T>C	XP_005248576.2:p.Leu745Ser
XM_011543406.1:c.2357T>C	XP_011541708.1:p.Leu786Ser
XM_011543407.1:c.2333T>C	XP_011541709.1:p.Leu778Ser
XM_011543408.1:c.2612T>C	XP_011541710.1:p.Leu871Ser
XM_017009484.1:c.2201T>C	XP_016864973.1:p.Leu734Ser
XM_017009485.1:c.2123T>C	XP_016864974.1:p.Leu708Ser
XR_001742068.2:n.2643T>C
NM_005921.2:c.2612T>C MANE Select	NP_005912.1:p.Leu871Ser