Canonical Allele Identifier: CA7019770

Gene: ABCC4

Linked Data

• dbSNP Id: rs763550083
• ExAC: 13:95862932 G / C
• gnomAD v2: 13-95862932-G-C
• gnomAD v4: 13-95210678-G-C
• MyVariant Identifiers: chr13:g.95862932G>C (hg19) ; chr13:g.95210678G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95210678G>C , CM000675.2:g.95210678G>C	GRCh38
NC_000013.10:g.95862932G>C , CM000675.1:g.95862932G>C	GRCh37
NC_000013.9:g.94660933G>C	NCBI36
NG_050651.1:g.95769C>G
NG_050651.2:g.95769C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000642524.1:c.*654+14C>G	ENSP00000493766.1:n.*654+14C>G
ENST00000643051.1:c.621+14C>G	ENSP00000495513.1:n.621+14C>G
ENST00000643556.1:c.762+14C>G	ENSP00000494938.1:n.762+14C>G
ENST00000643816.1:n.904+14C>G
ENST00000643842.1:c.*667+14C>G	ENSP00000493861.1:n.*667+14C>G
ENST00000644471.1:n.717+14C>G
ENST00000645237.2:c.621+14C>G MANE Select	ENSP00000494609.1:n.621+14C>G
ENST00000645532.1:c.660+14C>G	ENSP00000494431.1:n.660+14C>G
ENST00000646439.1:c.621+14C>G	ENSP00000494751.1:n.621+14C>G
ENST00000376887.8:c.621+14C>G	ENSP00000366084.4:n.621+14C>G
ENST00000536256.3:c.396+14C>G	ENSP00000442024.1:n.396+14C>G
ENST00000629385.1:c.621+14C>G	ENSP00000487081.1:n.621+14C>G
NM_001105515.2:c.621+14C>G	NP_001098985.1:n.621+14C>G
NM_001301829.1:c.621+14C>G	NP_001288758.1:n.621+14C>G
NM_001301830.1:c.396+14C>G	NP_001288759.1:n.396+14C>G
NM_005845.4:c.621+14C>G	NP_005836.2:n.621+14C>G
XM_005254025.2:c.492+14C>G	XP_005254082.1:n.492+14C>G
XM_006719914.1:c.621+14C>G	XP_006719977.1:n.621+14C>G
XM_011521047.1:c.72+14C>G	XP_011519349.1:n.72+14C>G
XM_017020319.1:c.492+14C>G	XP_016875808.1:n.492+14C>G
XM_017020320.2:c.621+14C>G	XP_016875809.1:n.621+14C>G
XM_017020322.1:c.492+14C>G	XP_016875811.1:n.492+14C>G
NM_001105515.3:c.621+14C>G	NP_001098985.1:n.621+14C>G
NM_001301829.2:c.621+14C>G	NP_001288758.1:n.621+14C>G
NM_001301830.2:c.396+14C>G	NP_001288759.1:n.396+14C>G
NM_005845.5:c.621+14C>G MANE Select	NP_005836.2:n.621+14C>G