Canonical Allele Identifier: CA359787802

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178193A>C (hg19) ; chr5:g.56882366A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882366A>C , CM000667.2:g.56882366A>C	GRCh38
NC_000005.9:g.56178193A>C , CM000667.1:g.56178193A>C	GRCh37
NC_000005.8:g.56213950A>C	NCBI36
NG_031884.1:g.72294A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3166A>C MANE Select	ENSP00000382423.3:p.Asn1056His
ENST00000399503.3:c.3166A>C	ENSP00000382423.3:p.Asn1056His
NM_005921.1:c.3166A>C	NP_005912.1:p.Asn1056His
XM_005248519.3:c.2788A>C	XP_005248576.2:p.Asn930His
XM_011543406.1:c.2911A>C	XP_011541708.1:p.Asn971His
XM_011543407.1:c.2887A>C	XP_011541709.1:p.Asn963His
XM_011543408.1:c.3166A>C	XP_011541710.1:p.Asn1056His
XM_017009484.1:c.2755A>C	XP_016864973.1:p.Asn919His
XM_017009485.1:c.2677A>C	XP_016864974.1:p.Asn893His
XR_001742068.2:n.3197A>C
NM_005921.2:c.3166A>C MANE Select	NP_005912.1:p.Asn1056His