Canonical Allele Identifier: CA2728849078
Gene: ABCC4 HGNC NCBI

Linked Data

dbSNP Id: rs2139574565

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.95171056_95171057insA , CM000675.2:g.95171056_95171057insA GRCh38
NC_000013.10:g.95823310_95823311insA , CM000675.1:g.95823310_95823311insA GRCh37
NC_000013.9:g.94621311_94621312insA NCBI36
NG_050651.1:g.135390_135391insT
NG_050651.2:g.135390_135391insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000642524.1:c.*1761-429_*1761-428insT ENSP00000493766.1:n.*1761-429_*1761-428insT
ENST00000643051.1:c.1728-429_1728-428insT ENSP00000495513.1:n.1728-429_1728-428insT
ENST00000643556.1:c.1869-429_1869-428insT ENSP00000494938.1:n.1869-429_1869-428insT
ENST00000643816.1:n.2011-429_2011-428insT
ENST00000643842.1:c.*1774-429_*1774-428insT ENSP00000493861.1:n.*1774-429_*1774-428insT
ENST00000644471.1:n.1819-429_1819-428insT
ENST00000645237.2:c.1728-429_1728-428insT MANE Select ENSP00000494609.1:n.1728-429_1728-428insT
ENST00000645532.1:c.1767-429_1767-428insT ENSP00000494431.1:n.1767-429_1767-428insT
ENST00000646439.1:c.1728-429_1728-428insT ENSP00000494751.1:n.1728-429_1728-428insT
ENST00000376887.8:c.1728-429_1728-428insT ENSP00000366084.4:n.1728-429_1728-428insT
ENST00000536256.3:c.1503-429_1503-428insT ENSP00000442024.1:n.1503-429_1503-428insT
ENST00000629385.1:c.1728-429_1728-428insT ENSP00000487081.1:n.1728-429_1728-428insT
NM_001105515.2:c.1728-429_1728-428insT NP_001098985.1:n.1728-429_1728-428insT
NM_001301829.1:c.1728-429_1728-428insT NP_001288758.1:n.1728-429_1728-428insT
NM_001301830.1:c.1503-429_1503-428insT NP_001288759.1:n.1503-429_1503-428insT
NM_005845.4:c.1728-429_1728-428insT NP_005836.2:n.1728-429_1728-428insT
XM_005254025.2:c.1599-429_1599-428insT XP_005254082.1:n.1599-429_1599-428insT
XM_006719914.1:c.1638-429_1638-428insT XP_006719977.1:n.1638-429_1638-428insT
XM_011521047.1:c.1179-429_1179-428insT XP_011519349.1:n.1179-429_1179-428insT
XM_017020319.1:c.1599-429_1599-428insT XP_016875808.1:n.1599-429_1599-428insT
XM_017020320.2:c.1728-429_1728-428insT XP_016875809.1:n.1728-429_1728-428insT
XM_017020321.1:c.213-429_213-428insT XP_016875810.1:n.213-429_213-428insT
XM_017020322.1:c.1599-429_1599-428insT XP_016875811.1:n.1599-429_1599-428insT
NM_001105515.3:c.1728-429_1728-428insT NP_001098985.1:n.1728-429_1728-428insT
NM_001301829.2:c.1728-429_1728-428insT NP_001288758.1:n.1728-429_1728-428insT
NM_001301830.2:c.1503-429_1503-428insT NP_001288759.1:n.1503-429_1503-428insT
NM_005845.5:c.1728-429_1728-428insT MANE Select NP_005836.2:n.1728-429_1728-428insT