Canonical Allele Identifier: CA2673909485

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56875458-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875459_56875460del , CM000667.2:g.56875459_56875460del	GRCh38
NC_000005.9:g.56171286_56171287del , CM000667.1:g.56171286_56171287del	GRCh37
NC_000005.8:g.56207043_56207044del	NCBI36
NG_031884.1:g.65387_65388del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+149_1965+150del MANE Select	ENSP00000382423.3:n.1965+149_1965+150del
ENST00000399503.3:c.1965+149_1965+150del	ENSP00000382423.3:n.1965+149_1965+150del
NM_005921.1:c.1965+149_1965+150del	NP_005912.1:n.1965+149_1965+150del
XM_005248519.3:c.1587+149_1587+150del	XP_005248576.2:n.1587+149_1587+150del
XM_011543406.1:c.1710+149_1710+150del	XP_011541708.1:n.1710+149_1710+150del
XM_011543407.1:c.1686+2454_1686+2455del	XP_011541709.1:n.1686+2454_1686+2455del
XM_011543408.1:c.1965+149_1965+150del	XP_011541710.1:n.1965+149_1965+150del
XM_017009484.1:c.1554+149_1554+150del	XP_016864973.1:n.1554+149_1554+150del
XM_017009485.1:c.1476+149_1476+150del	XP_016864974.1:n.1476+149_1476+150del
XR_001742068.2:n.1996+149_1996+150del
NM_005921.2:c.1965+149_1965+150del MANE Select	NP_005912.1:n.1965+149_1965+150del