Canonical Allele Identifier: CA359787873

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178227C>A (hg19) ; chr5:g.56882400C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882400C>A , CM000667.2:g.56882400C>A	GRCh38
NC_000005.9:g.56178227C>A , CM000667.1:g.56178227C>A	GRCh37
NC_000005.8:g.56213984C>A	NCBI36
NG_031884.1:g.72328C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3200C>A MANE Select	ENSP00000382423.3:p.Pro1067Gln
ENST00000399503.3:c.3200C>A	ENSP00000382423.3:p.Pro1067Gln
NM_005921.1:c.3200C>A	NP_005912.1:p.Pro1067Gln
XM_005248519.3:c.2822C>A	XP_005248576.2:p.Pro941Gln
XM_011543406.1:c.2945C>A	XP_011541708.1:p.Pro982Gln
XM_011543407.1:c.2921C>A	XP_011541709.1:p.Pro974Gln
XM_011543408.1:c.3200C>A	XP_011541710.1:p.Pro1067Gln
XM_017009484.1:c.2789C>A	XP_016864973.1:p.Pro930Gln
XM_017009485.1:c.2711C>A	XP_016864974.1:p.Pro904Gln
XR_001742068.2:n.3231C>A
NM_005921.2:c.3200C>A MANE Select	NP_005912.1:p.Pro1067Gln