Canonical Allele Identifier: CA388400196

Gene: ABCC4

Linked Data

• gnomAD v4: 13-95170557-G-A
• MyVariant Identifiers: chr13:g.95822811G>A (hg19) ; chr13:g.95170557G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95170557G>A , CM000675.2:g.95170557G>A	GRCh38
NC_000013.10:g.95822811G>A , CM000675.1:g.95822811G>A	GRCh37
NC_000013.9:g.94620812G>A	NCBI36
NG_050651.1:g.135890C>T
NG_050651.2:g.135890C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*1832C>T	ENSP00000493766.1:n.*1832C>T
ENST00000643051.1:c.1799C>T	ENSP00000495513.1:p.Ala600Val
ENST00000643556.1:c.1940C>T	ENSP00000494938.1:n.1940C>T
ENST00000643816.1:n.2082C>T
ENST00000643842.1:c.*1845C>T	ENSP00000493861.1:n.*1845C>T
ENST00000644471.1:n.1890C>T
ENST00000645237.2:c.1799C>T MANE Select	ENSP00000494609.1:p.Ala600Val
ENST00000645532.1:c.1838C>T	ENSP00000494431.1:p.Ala613Val
ENST00000646439.1:c.1799C>T	ENSP00000494751.1:p.Ala600Val
ENST00000376887.8:c.1799C>T	ENSP00000366084.4:p.Ala600Val
ENST00000536256.3:c.1574C>T	ENSP00000442024.1:p.Ala525Val
ENST00000629385.1:c.1799C>T	ENSP00000487081.1:p.Ala600Val
NM_001105515.2:c.1799C>T	NP_001098985.1:p.Ala600Val
NM_001301829.1:c.1799C>T	NP_001288758.1:p.Ala600Val
NM_001301830.1:c.1574C>T	NP_001288759.1:p.Ala525Val
NM_005845.4:c.1799C>T	NP_005836.2:p.Ala600Val
XM_005254025.2:c.1670C>T	XP_005254082.1:p.Ala557Val
XM_006719914.1:c.1709C>T	XP_006719977.1:p.Ala570Val
XM_011521047.1:c.1250C>T	XP_011519349.1:p.Ala417Val
XM_017020319.1:c.1670C>T	XP_016875808.1:p.Ala557Val
XM_017020320.2:c.1799C>T	XP_016875809.1:p.Ala600Val
XM_017020321.1:c.284C>T	XP_016875810.1:p.Ala95Val
XM_017020322.1:c.1670C>T	XP_016875811.1:p.Ala557Val
NM_001105515.3:c.1799C>T	NP_001098985.1:p.Ala600Val
NM_001301829.2:c.1799C>T	NP_001288758.1:p.Ala600Val
NM_001301830.2:c.1574C>T	NP_001288759.1:p.Ala525Val
NM_005845.5:c.1799C>T MANE Select	NP_005836.2:p.Ala600Val