Canonical Allele Identifier: CA359787864

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56882394-C-T
• MyVariant Identifiers: chr5:g.56178221C>T (hg19) ; chr5:g.56882394C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882394C>T , CM000667.2:g.56882394C>T	GRCh38
NC_000005.9:g.56178221C>T , CM000667.1:g.56178221C>T	GRCh37
NC_000005.8:g.56213978C>T	NCBI36
NG_031884.1:g.72322C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3194C>T MANE Select	ENSP00000382423.3:p.Pro1065Leu
ENST00000399503.3:c.3194C>T	ENSP00000382423.3:p.Pro1065Leu
NM_005921.1:c.3194C>T	NP_005912.1:p.Pro1065Leu
XM_005248519.3:c.2816C>T	XP_005248576.2:p.Pro939Leu
XM_011543406.1:c.2939C>T	XP_011541708.1:p.Pro980Leu
XM_011543407.1:c.2915C>T	XP_011541709.1:p.Pro972Leu
XM_011543408.1:c.3194C>T	XP_011541710.1:p.Pro1065Leu
XM_017009484.1:c.2783C>T	XP_016864973.1:p.Pro928Leu
XM_017009485.1:c.2705C>T	XP_016864974.1:p.Pro902Leu
XR_001742068.2:n.3225C>T
NM_005921.2:c.3194C>T MANE Select	NP_005912.1:p.Pro1065Leu