Canonical Allele Identifier: CA1076340697

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1747995820
• gnomAD v3: 5-56875471-G-GTTTA
• gnomAD v4: 5-56875471-G-GTTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875475_56875478dup , CM000667.2:g.56875475_56875478dup	GRCh38
NC_000005.9:g.56171302_56171305dup , CM000667.1:g.56171302_56171305dup	GRCh37
NC_000005.8:g.56207059_56207062dup	NCBI36
NG_031884.1:g.65403_65406dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+165_1965+168dup MANE Select	ENSP00000382423.3:n.1965+165_1965+168dup
ENST00000399503.3:c.1965+165_1965+168dup	ENSP00000382423.3:n.1965+165_1965+168dup
NM_005921.1:c.1965+165_1965+168dup	NP_005912.1:n.1965+165_1965+168dup
XM_005248519.3:c.1587+165_1587+168dup	XP_005248576.2:n.1587+165_1587+168dup
XM_011543406.1:c.1710+165_1710+168dup	XP_011541708.1:n.1710+165_1710+168dup
XM_011543407.1:c.1686+2470_1686+2473dup	XP_011541709.1:n.1686+2470_1686+2473dup
XM_011543408.1:c.1965+165_1965+168dup	XP_011541710.1:n.1965+165_1965+168dup
XM_017009484.1:c.1554+165_1554+168dup	XP_016864973.1:n.1554+165_1554+168dup
XM_017009485.1:c.1476+165_1476+168dup	XP_016864974.1:n.1476+165_1476+168dup
XR_001742068.2:n.1996+165_1996+168dup
NM_005921.2:c.1965+165_1965+168dup MANE Select	NP_005912.1:n.1965+165_1965+168dup