Canonical Allele Identifier: CA388400200

Gene: ABCC4

Linked Data

• dbSNP Id: rs2037432594
• gnomAD v4: 13-95170560-G-A
• MyVariant Identifiers: chr13:g.95822814G>A (hg19) ; chr13:g.95170560G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95170560G>A , CM000675.2:g.95170560G>A	GRCh38
NC_000013.10:g.95822814G>A , CM000675.1:g.95822814G>A	GRCh37
NC_000013.9:g.94620815G>A	NCBI36
NG_050651.1:g.135887C>T
NG_050651.2:g.135887C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*1829C>T	ENSP00000493766.1:n.*1829C>T
ENST00000643051.1:c.1796C>T	ENSP00000495513.1:p.Ala599Val
ENST00000643556.1:c.1937C>T	ENSP00000494938.1:n.1937C>T
ENST00000643816.1:n.2079C>T
ENST00000643842.1:c.*1842C>T	ENSP00000493861.1:n.*1842C>T
ENST00000644471.1:n.1887C>T
ENST00000645237.2:c.1796C>T MANE Select	ENSP00000494609.1:p.Ala599Val
ENST00000645532.1:c.1835C>T	ENSP00000494431.1:p.Ala612Val
ENST00000646439.1:c.1796C>T	ENSP00000494751.1:p.Ala599Val
ENST00000376887.8:c.1796C>T	ENSP00000366084.4:p.Ala599Val
ENST00000536256.3:c.1571C>T	ENSP00000442024.1:p.Ala524Val
ENST00000629385.1:c.1796C>T	ENSP00000487081.1:p.Ala599Val
NM_001105515.2:c.1796C>T	NP_001098985.1:p.Ala599Val
NM_001301829.1:c.1796C>T	NP_001288758.1:p.Ala599Val
NM_001301830.1:c.1571C>T	NP_001288759.1:p.Ala524Val
NM_005845.4:c.1796C>T	NP_005836.2:p.Ala599Val
XM_005254025.2:c.1667C>T	XP_005254082.1:p.Ala556Val
XM_006719914.1:c.1706C>T	XP_006719977.1:p.Ala569Val
XM_011521047.1:c.1247C>T	XP_011519349.1:p.Ala416Val
XM_017020319.1:c.1667C>T	XP_016875808.1:p.Ala556Val
XM_017020320.2:c.1796C>T	XP_016875809.1:p.Ala599Val
XM_017020321.1:c.281C>T	XP_016875810.1:p.Ala94Val
XM_017020322.1:c.1667C>T	XP_016875811.1:p.Ala556Val
NM_001105515.3:c.1796C>T	NP_001098985.1:p.Ala599Val
NM_001301829.2:c.1796C>T	NP_001288758.1:p.Ala599Val
NM_001301830.2:c.1571C>T	NP_001288759.1:p.Ala524Val
NM_005845.5:c.1796C>T MANE Select	NP_005836.2:p.Ala599Val