Canonical Allele Identifier: CA812363561

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1357645960
• MyVariant Identifiers: chr5:g.56153275A>T (hg19) ; chr5:g.56857448A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56857448A>T , CM000667.2:g.56857448A>T	GRCh38
NC_000005.9:g.56153275A>T , CM000667.1:g.56153275A>T	GRCh37
NC_000005.8:g.56189032A>T	NCBI36
NG_031884.1:g.47376A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.633+698A>T MANE Select	ENSP00000382423.3:n.633+698A>T
ENST00000399503.3:c.633+698A>T	ENSP00000382423.3:n.633+698A>T
NM_005921.1:c.633+698A>T	NP_005912.1:n.633+698A>T
XM_005248519.3:c.255+698A>T	XP_005248576.2:n.255+698A>T
XM_011543406.1:c.378+698A>T	XP_011541708.1:n.378+698A>T
XM_011543407.1:c.633+698A>T	XP_011541709.1:n.633+698A>T
XM_011543408.1:c.633+698A>T	XP_011541710.1:n.633+698A>T
XM_017009484.1:c.222+698A>T	XP_016864973.1:n.222+698A>T
XM_017009485.1:c.144+698A>T	XP_016864974.1:n.144+698A>T
XR_001742068.2:n.664+698A>T
NM_005921.2:c.633+698A>T MANE Select	NP_005912.1:n.633+698A>T