Canonical Allele Identifier: CA359786444

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1160631626
• MyVariant Identifiers: chr5:g.56177731C>A (hg19) ; chr5:g.56881904C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881904C>A , CM000667.2:g.56881904C>A	GRCh38
NC_000005.9:g.56177731C>A , CM000667.1:g.56177731C>A	GRCh37
NC_000005.8:g.56213488C>A	NCBI36
NG_031884.1:g.71832C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2704C>A MANE Select	ENSP00000382423.3:p.Pro902Thr
ENST00000399503.3:c.2704C>A	ENSP00000382423.3:p.Pro902Thr
NM_005921.1:c.2704C>A	NP_005912.1:p.Pro902Thr
XM_005248519.3:c.2326C>A	XP_005248576.2:p.Pro776Thr
XM_011543406.1:c.2449C>A	XP_011541708.1:p.Pro817Thr
XM_011543407.1:c.2425C>A	XP_011541709.1:p.Pro809Thr
XM_011543408.1:c.2704C>A	XP_011541710.1:p.Pro902Thr
XM_017009484.1:c.2293C>A	XP_016864973.1:p.Pro765Thr
XM_017009485.1:c.2215C>A	XP_016864974.1:p.Pro739Thr
XR_001742068.2:n.2735C>A
NM_005921.2:c.2704C>A MANE Select	NP_005912.1:p.Pro902Thr