Canonical Allele Identifier: CA254217631

Gene: ABCC4

Linked Data

• dbSNP Id: rs969471569
• MyVariant Identifiers: chr13:g.95874913G>A (hg19) ; chr13:g.95222659G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95222659G>A , CM000675.2:g.95222659G>A	GRCh38
NC_000013.10:g.95874913G>A , CM000675.1:g.95874913G>A	GRCh37
NC_000013.9:g.94672914G>A	NCBI36
NG_050651.1:g.83788C>T
NG_050651.2:g.83788C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*565-11878C>T	ENSP00000493766.1:n.*565-11878C>T
ENST00000643051.1:c.532-11878C>T	ENSP00000495513.1:n.532-11878C>T
ENST00000643556.1:c.673-11878C>T	ENSP00000494938.1:n.673-11878C>T
ENST00000643816.1:n.815-11878C>T
ENST00000643842.1:c.*578-11878C>T	ENSP00000493861.1:n.*578-11878C>T
ENST00000644471.1:n.628-11878C>T
ENST00000645237.2:c.532-11878C>T MANE Select	ENSP00000494609.1:n.532-11878C>T
ENST00000645532.1:c.571-11878C>T	ENSP00000494431.1:n.571-11878C>T
ENST00000646439.1:c.532-11878C>T	ENSP00000494751.1:n.532-11878C>T
ENST00000376887.8:c.532-11878C>T	ENSP00000366084.4:n.532-11878C>T
ENST00000536256.3:c.307-11878C>T	ENSP00000442024.1:n.307-11878C>T
ENST00000629385.1:c.532-11878C>T	ENSP00000487081.1:n.532-11878C>T
NM_001105515.2:c.532-11878C>T	NP_001098985.1:n.532-11878C>T
NM_001301829.1:c.532-11878C>T	NP_001288758.1:n.532-11878C>T
NM_001301830.1:c.307-11878C>T	NP_001288759.1:n.307-11878C>T
NM_005845.4:c.532-11878C>T	NP_005836.2:n.532-11878C>T
XM_005254025.2:c.403-11878C>T	XP_005254082.1:n.403-11878C>T
XM_006719914.1:c.532-11878C>T	XP_006719977.1:n.532-11878C>T
XM_017020319.1:c.403-11878C>T	XP_016875808.1:n.403-11878C>T
XM_017020320.2:c.532-11878C>T	XP_016875809.1:n.532-11878C>T
XM_017020322.1:c.403-11878C>T	XP_016875811.1:n.403-11878C>T
NM_001105515.3:c.532-11878C>T	NP_001098985.1:n.532-11878C>T
NM_001301829.2:c.532-11878C>T	NP_001288758.1:n.532-11878C>T
NM_001301830.2:c.307-11878C>T	NP_001288759.1:n.307-11878C>T
NM_005845.5:c.532-11878C>T MANE Select	NP_005836.2:n.532-11878C>T