Canonical Allele Identifier: CA559802753

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1245161979
• gnomAD v2: 5-56155757-C-T
• gnomAD v4: 5-56859930-C-T
• MyVariant Identifiers: chr5:g.56155757C>T (hg19) ; chr5:g.56859930C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859930C>T , CM000667.2:g.56859930C>T	GRCh38
NC_000005.9:g.56155757C>T , CM000667.1:g.56155757C>T	GRCh37
NC_000005.8:g.56191514C>T	NCBI36
NG_031884.1:g.49858C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.834+15C>T MANE Select	ENSP00000382423.3:n.834+15C>T
ENST00000399503.3:c.834+15C>T	ENSP00000382423.3:n.834+15C>T
NM_005921.1:c.834+15C>T	NP_005912.1:n.834+15C>T
XM_005248519.3:c.456+15C>T	XP_005248576.2:n.456+15C>T
XM_011543406.1:c.579+15C>T	XP_011541708.1:n.579+15C>T
XM_011543407.1:c.834+15C>T	XP_011541709.1:n.834+15C>T
XM_011543408.1:c.834+15C>T	XP_011541710.1:n.834+15C>T
XM_017009484.1:c.423+15C>T	XP_016864973.1:n.423+15C>T
XM_017009485.1:c.345+15C>T	XP_016864974.1:n.345+15C>T
XR_001742068.2:n.865+15C>T
NM_005921.2:c.834+15C>T MANE Select	NP_005912.1:n.834+15C>T