Canonical Allele Identifier: CA702615747

Gene: ABCC4

Linked Data

• dbSNP Id: rs113197872
• gnomAD v3: 13-95061669-T-TTA
• gnomAD v4: 13-95061669-T-TTA
• MyVariant Identifiers: chr13:g.95713923_95713924insTA (hg19) ; chr13:g.95061669_95061670insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95061669_95061670insTA , CM000675.2:g.95061669_95061670insTA	GRCh38
NC_000013.10:g.95713923_95713924insTA , CM000675.1:g.95713923_95713924insTA	GRCh37
NC_000013.9:g.94511924_94511925insTA	NCBI36
NG_050651.1:g.244777_244778insTA
NG_050651.2:g.244777_244778insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643051.1:c.*991+1034_*991+1035insTA	ENSP00000495513.1:n.*991+1034_*991+1035insTA
ENST00000643842.1:c.*3412+1034_*3412+1035insTA	ENSP00000493861.1:n.*3412+1034_*3412+1035insTA
ENST00000645237.2:c.3366+1034_3366+1035insTA MANE Select	ENSP00000494609.1:n.3366+1034_3366+1035insTA
ENST00000646439.1:c.3225+1034_3225+1035insTA	ENSP00000494751.1:n.3225+1034_3225+1035insTA
ENST00000376887.8:c.3366+1034_3366+1035insTA	ENSP00000366084.4:n.3366+1034_3366+1035insTA
NM_001301829.1:c.3225+1034_3225+1035insTA	NP_001288758.1:n.3225+1034_3225+1035insTA
NM_005845.4:c.3366+1034_3366+1035insTA	NP_005836.2:n.3366+1034_3366+1035insTA
XM_005254025.2:c.3237+1034_3237+1035insTA	XP_005254082.1:n.3237+1034_3237+1035insTA
XM_006719914.1:c.3276+1034_3276+1035insTA	XP_006719977.1:n.3276+1034_3276+1035insTA
XM_011521047.1:c.2817+1034_2817+1035insTA	XP_011519349.1:n.2817+1034_2817+1035insTA
XM_017020319.1:c.3237+1034_3237+1035insTA	XP_016875808.1:n.3237+1034_3237+1035insTA
XM_017020321.1:c.1851+1034_1851+1035insTA	XP_016875810.1:n.1851+1034_1851+1035insTA
NM_001301829.2:c.3225+1034_3225+1035insTA	NP_001288758.1:n.3225+1034_3225+1035insTA
NM_005845.5:c.3366+1034_3366+1035insTA MANE Select	NP_005836.2:n.3366+1034_3366+1035insTA