Canonical Allele Identifier: CA359780694

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56170938A>C (hg19) ; chr5:g.56875111A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875111A>C , CM000667.2:g.56875111A>C	GRCh38
NC_000005.9:g.56170938A>C , CM000667.1:g.56170938A>C	GRCh37
NC_000005.8:g.56206695A>C	NCBI36
NG_031884.1:g.65039A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1766A>C MANE Select	ENSP00000382423.3:p.His589Pro
ENST00000399503.3:c.1766A>C	ENSP00000382423.3:p.His589Pro
NM_005921.1:c.1766A>C	NP_005912.1:p.His589Pro
XM_005248519.3:c.1388A>C	XP_005248576.2:p.His463Pro
XM_011543406.1:c.1511A>C	XP_011541708.1:p.His504Pro
XM_011543407.1:c.1686+2106A>C	XP_011541709.1:n.1686+2106A>C
XM_011543408.1:c.1766A>C	XP_011541710.1:p.His589Pro
XM_017009484.1:c.1355A>C	XP_016864973.1:p.His452Pro
XM_017009485.1:c.1277A>C	XP_016864974.1:p.His426Pro
XR_001742068.2:n.1797A>C
NM_005921.2:c.1766A>C MANE Select	NP_005912.1:p.His589Pro