Canonical Allele Identifier: CA119520073

Gene: MAP3K1

Linked Data

• dbSNP Id: rs373481385
• gnomAD v4: 5-56859756-G-T
• MyVariant Identifiers: chr5:g.56155583G>T (hg19) ; chr5:g.56859756G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859756G>T , CM000667.2:g.56859756G>T	GRCh38
NC_000005.9:g.56155583G>T , CM000667.1:g.56155583G>T	GRCh37
NC_000005.8:g.56191340G>T	NCBI36
NG_031884.1:g.49684G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.675G>T MANE Select	ENSP00000382423.3:p.Met225Ile
ENST00000399503.3:c.675G>T	ENSP00000382423.3:p.Met225Ile
NM_005921.1:c.675G>T	NP_005912.1:p.Met225Ile
XM_005248519.3:c.297G>T	XP_005248576.2:p.Met99Ile
XM_011543406.1:c.420G>T	XP_011541708.1:p.Met140Ile
XM_011543407.1:c.675G>T	XP_011541709.1:p.Met225Ile
XM_011543408.1:c.675G>T	XP_011541710.1:p.Met225Ile
XM_017009484.1:c.264G>T	XP_016864973.1:p.Met88Ile
XM_017009485.1:c.186G>T	XP_016864974.1:p.Met62Ile
XR_001742068.2:n.706G>T
NM_005921.2:c.675G>T MANE Select	NP_005912.1:p.Met225Ile