Canonical Allele Identifier: CA559801340

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1179587314
• gnomAD v2: 5-56177367-TATATG-T
• gnomAD v3: 5-56881540-TATATG-T
• gnomAD v4: 5-56881540-TATATG-T
• MyVariant Identifiers: chr5:g.56177368_56177372del (hg19) ; chr5:g.56881541_56881545del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881541_56881545del , CM000667.2:g.56881541_56881545del	GRCh38
NC_000005.9:g.56177368_56177372del , CM000667.1:g.56177368_56177372del	GRCh37
NC_000005.8:g.56213125_56213129del	NCBI36
NG_031884.1:g.71469_71473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2370-29_2370-25del MANE Select	ENSP00000382423.3:n.2370-29_2370-25del
ENST00000399503.3:c.2370-29_2370-25del	ENSP00000382423.3:n.2370-29_2370-25del
NM_005921.1:c.2370-29_2370-25del	NP_005912.1:n.2370-29_2370-25del
XM_005248519.3:c.1992-29_1992-25del	XP_005248576.2:n.1992-29_1992-25del
XM_011543406.1:c.2115-29_2115-25del	XP_011541708.1:n.2115-29_2115-25del
XM_011543407.1:c.2091-29_2091-25del	XP_011541709.1:n.2091-29_2091-25del
XM_011543408.1:c.2370-29_2370-25del	XP_011541710.1:n.2370-29_2370-25del
XM_017009484.1:c.1959-29_1959-25del	XP_016864973.1:n.1959-29_1959-25del
XM_017009485.1:c.1881-29_1881-25del	XP_016864974.1:n.1881-29_1881-25del
XR_001742068.2:n.2401-29_2401-25del
NM_005921.2:c.2370-29_2370-25del MANE Select	NP_005912.1:n.2370-29_2370-25del