Canonical Allele Identifier: CA1057203576
Gene: ABCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1716621252

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183960541C>T , CM000665.2:g.183960541C>T GRCh38
NC_000003.11:g.183678329C>T , CM000665.1:g.183678329C>T GRCh37
NC_000003.10:g.185161023C>T NCBI36
NG_047115.1:g.62470G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334444.11:c.2380-706G>A MANE Select ENSP00000333926.6:n.2380-706G>A
ENST00000265586.10:c.2380-706G>A ENSP00000265586.6:n.2380-706G>A
ENST00000334444.10:c.2380-706G>A ENSP00000333926.6:n.2380-706G>A
ENST00000437205.5:c.*1073-706G>A ENSP00000403510.1:n.*1073-706G>A
NM_005688.2:c.2380-706G>A NP_005679.2:n.2380-706G>A
XM_005247058.3:c.2380-706G>A XP_005247115.1:n.2380-706G>A
XM_005247059.3:c.2380-706G>A XP_005247116.1:n.2380-706G>A
XM_011512314.1:c.2380-706G>A XP_011510616.1:n.2380-706G>A
XM_011512315.1:c.2380-706G>A XP_011510617.1:n.2380-706G>A
XM_011512316.1:c.964-706G>A XP_011510618.1:n.964-706G>A
NM_001320032.1:c.964-706G>A NP_001306961.1:n.964-706G>A
NM_005688.3:c.2380-706G>A NP_005679.2:n.2380-706G>A
XM_005247058.5:c.2380-706G>A XP_005247115.1:n.2380-706G>A
XM_005247059.5:c.2380-706G>A XP_005247116.1:n.2380-706G>A
XM_011512314.2:c.2380-706G>A XP_011510616.1:n.2380-706G>A
XM_017005492.2:c.1846-706G>A XP_016860981.1:n.1846-706G>A
XM_024453286.1:c.1846-706G>A XP_024309054.1:n.1846-706G>A
NM_005688.4:c.2380-706G>A MANE Select NP_005679.2:n.2380-706G>A
NM_001320032.2:c.964-706G>A NP_001306961.1:n.964-706G>A