Canonical Allele Identifier: CA359785764

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177449T>C (hg19) ; chr5:g.56881622T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881622T>C , CM000667.2:g.56881622T>C	GRCh38
NC_000005.9:g.56177449T>C , CM000667.1:g.56177449T>C	GRCh37
NC_000005.8:g.56213206T>C	NCBI36
NG_031884.1:g.71550T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2422T>C MANE Select	ENSP00000382423.3:p.Ser808Pro
ENST00000399503.3:c.2422T>C	ENSP00000382423.3:p.Ser808Pro
NM_005921.1:c.2422T>C	NP_005912.1:p.Ser808Pro
XM_005248519.3:c.2044T>C	XP_005248576.2:p.Ser682Pro
XM_011543406.1:c.2167T>C	XP_011541708.1:p.Ser723Pro
XM_011543407.1:c.2143T>C	XP_011541709.1:p.Ser715Pro
XM_011543408.1:c.2422T>C	XP_011541710.1:p.Ser808Pro
XM_017009484.1:c.2011T>C	XP_016864973.1:p.Ser671Pro
XM_017009485.1:c.1933T>C	XP_016864974.1:p.Ser645Pro
XR_001742068.2:n.2453T>C
NM_005921.2:c.2422T>C MANE Select	NP_005912.1:p.Ser808Pro