Canonical Allele Identifier: CA359787615

Gene: MAP3K1

Linked Data

• dbSNP Id: rs3822625
• MyVariant Identifiers: chr5:g.56178111A>C (hg19) ; chr5:g.56882284A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882284A>C , CM000667.2:g.56882284A>C	GRCh38
NC_000005.9:g.56178111A>C , CM000667.1:g.56178111A>C	GRCh37
NC_000005.8:g.56213868A>C	NCBI36
NG_031884.1:g.72212A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3084A>C MANE Select	ENSP00000382423.3:p.Gln1028His
ENST00000399503.3:c.3084A>C	ENSP00000382423.3:p.Gln1028His
NM_005921.1:c.3084A>C	NP_005912.1:p.Gln1028His
XM_005248519.3:c.2706A>C	XP_005248576.2:p.Gln902His
XM_011543406.1:c.2829A>C	XP_011541708.1:p.Gln943His
XM_011543407.1:c.2805A>C	XP_011541709.1:p.Gln935His
XM_011543408.1:c.3084A>C	XP_011541710.1:p.Gln1028His
XM_017009484.1:c.2673A>C	XP_016864973.1:p.Gln891His
XM_017009485.1:c.2595A>C	XP_016864974.1:p.Gln865His
XR_001742068.2:n.3115A>C
NM_005921.2:c.3084A>C MANE Select	NP_005912.1:p.Gln1028His