Canonical Allele Identifier: CA359802610

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1156818215
• gnomAD v2: 5-56155689-A-T
• gnomAD v4: 5-56859862-A-T
• MyVariant Identifiers: chr5:g.56155689A>T (hg19) ; chr5:g.56859862A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859862A>T , CM000667.2:g.56859862A>T	GRCh38
NC_000005.9:g.56155689A>T , CM000667.1:g.56155689A>T	GRCh37
NC_000005.8:g.56191446A>T	NCBI36
NG_031884.1:g.49790A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.781A>T MANE Select	ENSP00000382423.3:p.Thr261Ser
ENST00000399503.3:c.781A>T	ENSP00000382423.3:p.Thr261Ser
NM_005921.1:c.781A>T	NP_005912.1:p.Thr261Ser
XM_005248519.3:c.403A>T	XP_005248576.2:p.Thr135Ser
XM_011543406.1:c.526A>T	XP_011541708.1:p.Thr176Ser
XM_011543407.1:c.781A>T	XP_011541709.1:p.Thr261Ser
XM_011543408.1:c.781A>T	XP_011541710.1:p.Thr261Ser
XM_017009484.1:c.370A>T	XP_016864973.1:p.Thr124Ser
XM_017009485.1:c.292A>T	XP_016864974.1:p.Thr98Ser
XR_001742068.2:n.812A>T
NM_005921.2:c.781A>T MANE Select	NP_005912.1:p.Thr261Ser