Canonical Allele Identifier: CA319205709

Gene: MAP3K7CL

Linked Data

• dbSNP Id: rs2832191
• gnomAD v2: 21-30489300-A-C
• gnomAD v3: 21-29116979-A-C
• gnomAD v4: 21-29116979-A-C
• MyVariant Identifiers: chr21:g.30489300A>C (hg19) ; chr21:g.29116979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.29116979A>C , CM000683.2:g.29116979A>C	GRCh38
NC_000021.8:g.30489300A>C , CM000683.1:g.30489300A>C	GRCh37
NC_000021.7:g.29411171A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710354.1:c.*139+7796A>C	ENSP00000518225.1:n.*139+7796A>C
ENST00000286791.9:c.370+24398A>C	ENSP00000286791.6:n.370+24398A>C
ENST00000339024.8:c.-169+7796A>C	ENSP00000345777.4:n.-169+7796A>C
ENST00000341618.8:c.370+24398A>C	ENSP00000343212.4:n.370+24398A>C
ENST00000399934.5:c.-39-16327A>C	ENSP00000382816.1:n.-39-16327A>C
ENST00000399935.6:c.-168-13816A>C	ENSP00000382817.2:n.-168-13816A>C
ENST00000399947.6:c.370+24398A>C	ENSP00000382828.2:n.370+24398A>C
ENST00000545939.5:c.52+7796A>C	ENSP00000437846.1:n.52+7796A>C
NM_001286617.1:c.-168-13816A>C	NP_001273546.1:n.-168-13816A>C
NM_001286618.1:c.-39-16327A>C	NP_001273547.1:n.-39-16327A>C
NM_001286619.1:c.-169+7796A>C	NP_001273548.1:n.-169+7796A>C
NM_001286622.1:c.52+7796A>C	NP_001273551.1:n.52+7796A>C
NM_001286634.1:c.370+24398A>C	NP_001273563.1:n.370+24398A>C
NM_020152.3:c.370+24398A>C	NP_064537.1:n.370+24398A>C
NM_001286617.2:c.-168-13816A>C	NP_001273546.1:n.-168-13816A>C
NM_001286618.2:c.-39-16327A>C	NP_001273547.1:n.-39-16327A>C
NM_001286622.2:c.52+7796A>C	NP_001273551.1:n.52+7796A>C
NM_001286634.2:c.370+24398A>C	NP_001273563.1:n.370+24398A>C
NM_001371369.1:c.370+24398A>C	NP_001358298.1:n.370+24398A>C
NM_001371374.1:c.-169+7796A>C	NP_001358303.1:n.-169+7796A>C
NM_020152.4:c.370+24398A>C	NP_064537.1:n.370+24398A>C
NM_001286619.2:c.-169+7796A>C	NP_001273548.1:n.-169+7796A>C