Canonical Allele Identifier: CA2385049463

Gene: MAP3K7CL

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.29116899T= , CM000683.2:g.29116899T=	GRCh38
NC_000021.8:g.30489220T= , CM000683.1:g.30489220T=	GRCh37
NC_000021.7:g.29411091T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710354.1:c.*139+7716T=	ENSP00000518225.1:n.*139+7716T=
ENST00000286791.9:c.370+24318T=	ENSP00000286791.6:n.370+24318T=
ENST00000339024.8:c.-169+7716T=	ENSP00000345777.4:n.-169+7716T=
ENST00000341618.8:c.370+24318T=	ENSP00000343212.4:n.370+24318T=
ENST00000399934.5:c.-39-16407T=	ENSP00000382816.1:n.-39-16407T=
ENST00000399935.6:c.-168-13896T=	ENSP00000382817.2:n.-168-13896T=
ENST00000399947.6:c.370+24318T=	ENSP00000382828.2:n.370+24318T=
ENST00000545939.5:c.52+7716T=	ENSP00000437846.1:n.52+7716T=
NM_001286617.1:c.-168-13896T=	NP_001273546.1:n.-168-13896T=
NM_001286618.1:c.-39-16407T=	NP_001273547.1:n.-39-16407T=
NM_001286619.1:c.-169+7716T=	NP_001273548.1:n.-169+7716T=
NM_001286622.1:c.52+7716T=	NP_001273551.1:n.52+7716T=
NM_001286634.1:c.370+24318T=	NP_001273563.1:n.370+24318T=
NM_020152.3:c.370+24318T=	NP_064537.1:n.370+24318T=
NM_001286617.2:c.-168-13896T=	NP_001273546.1:n.-168-13896T=
NM_001286618.2:c.-39-16407T=	NP_001273547.1:n.-39-16407T=
NM_001286622.2:c.52+7716T=	NP_001273551.1:n.52+7716T=
NM_001286634.2:c.370+24318T=	NP_001273563.1:n.370+24318T=
NM_001371369.1:c.370+24318T=	NP_001358298.1:n.370+24318T=
NM_001371374.1:c.-169+7716T=	NP_001358303.1:n.-169+7716T=
NM_020152.4:c.370+24318T=	NP_064537.1:n.370+24318T=
NM_001286619.2:c.-169+7716T=	NP_001273548.1:n.-169+7716T=