Canonical Allele Identifier: CA388402569

Gene: ABCC4

Linked Data

• gnomAD v4: 13-95186699-A-G
• MyVariant Identifiers: chr13:g.95838953A>G (hg19) ; chr13:g.95186699A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95186699A>G , CM000675.2:g.95186699A>G	GRCh38
NC_000013.10:g.95838953A>G , CM000675.1:g.95838953A>G	GRCh37
NC_000013.9:g.94636954A>G	NCBI36
NG_050651.1:g.119748T>C
NG_050651.2:g.119748T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000642524.1:c.*1578+2T>C	ENSP00000493766.1:n.*1578+2T>C
ENST00000643051.1:c.1545+2T>C	ENSP00000495513.1:n.1545+2T>C
ENST00000643556.1:c.1686+2T>C	ENSP00000494938.1:n.1686+2T>C
ENST00000643816.1:n.1828+2T>C
ENST00000643842.1:c.*1591+2T>C	ENSP00000493861.1:n.*1591+2T>C
ENST00000644471.1:n.1641+2T>C
ENST00000645237.2:c.1545+2T>C MANE Select	ENSP00000494609.1:n.1545+2T>C
ENST00000645532.1:c.1584+2T>C	ENSP00000494431.1:n.1584+2T>C
ENST00000646439.1:c.1545+2T>C	ENSP00000494751.1:n.1545+2T>C
ENST00000376887.8:c.1545+2T>C	ENSP00000366084.4:n.1545+2T>C
ENST00000536256.3:c.1320+2T>C	ENSP00000442024.1:n.1320+2T>C
ENST00000629385.1:c.1545+2T>C	ENSP00000487081.1:n.1545+2T>C
NM_001105515.2:c.1545+2T>C	NP_001098985.1:n.1545+2T>C
NM_001301829.1:c.1545+2T>C	NP_001288758.1:n.1545+2T>C
NM_001301830.1:c.1320+2T>C	NP_001288759.1:n.1320+2T>C
NM_005845.4:c.1545+2T>C	NP_005836.2:n.1545+2T>C
XM_005254025.2:c.1416+2T>C	XP_005254082.1:n.1416+2T>C
XM_006719914.1:c.1455+2T>C	XP_006719977.1:n.1455+2T>C
XM_011521047.1:c.996+2T>C	XP_011519349.1:n.996+2T>C
XM_017020319.1:c.1416+2T>C	XP_016875808.1:n.1416+2T>C
XM_017020320.2:c.1545+2T>C	XP_016875809.1:n.1545+2T>C
XM_017020322.1:c.1416+2T>C	XP_016875811.1:n.1416+2T>C
NM_001105515.3:c.1545+2T>C	NP_001098985.1:n.1545+2T>C
NM_001301829.2:c.1545+2T>C	NP_001288758.1:n.1545+2T>C
NM_001301830.2:c.1320+2T>C	NP_001288759.1:n.1320+2T>C
NM_005845.5:c.1545+2T>C MANE Select	NP_005836.2:n.1545+2T>C