Canonical Allele Identifier: CA359786572

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56881961-A-C
• MyVariant Identifiers: chr5:g.56177788A>C (hg19) ; chr5:g.56881961A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881961A>C , CM000667.2:g.56881961A>C	GRCh38
NC_000005.9:g.56177788A>C , CM000667.1:g.56177788A>C	GRCh37
NC_000005.8:g.56213545A>C	NCBI36
NG_031884.1:g.71889A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2761A>C MANE Select	ENSP00000382423.3:p.Ser921Arg
ENST00000399503.3:c.2761A>C	ENSP00000382423.3:p.Ser921Arg
NM_005921.1:c.2761A>C	NP_005912.1:p.Ser921Arg
XM_005248519.3:c.2383A>C	XP_005248576.2:p.Ser795Arg
XM_011543406.1:c.2506A>C	XP_011541708.1:p.Ser836Arg
XM_011543407.1:c.2482A>C	XP_011541709.1:p.Ser828Arg
XM_011543408.1:c.2761A>C	XP_011541710.1:p.Ser921Arg
XM_017009484.1:c.2350A>C	XP_016864973.1:p.Ser784Arg
XM_017009485.1:c.2272A>C	XP_016864974.1:p.Ser758Arg
XR_001742068.2:n.2792A>C
NM_005921.2:c.2761A>C MANE Select	NP_005912.1:p.Ser921Arg