Canonical Allele Identifier: CA2658838252

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43878120-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43878122del , CM000664.2:g.43878122del	GRCh38
NC_000002.11:g.44105261del , CM000664.1:g.44105261del	GRCh37
NC_000002.10:g.43958765del	NCBI36
NG_008884.1:g.44159del
NG_008884.2:g.51181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.*209del MANE Select	ENSP00000272286.2:n.*209del
ENST00000272286.2:c.*209del	ENSP00000272286.2:n.*209del
NM_022437.2:c.*209del	NP_071882.1:n.*209del
XM_005264483.2:c.*209del	XP_005264540.1:n.*209del
XM_011533029.1:c.*209del	XP_011531331.1:n.*209del
XM_011533030.1:c.*209del	XP_011531332.1:n.*209del
XM_011533031.1:c.*209del	XP_011531333.1:n.*209del
XR_939707.1:n.2733del
NM_001357321.1:c.*209del	NP_001344250.1:n.*209del
XM_011533029.2:c.*209del	XP_011531331.1:n.*209del
XM_011533030.2:c.*209del	XP_011531332.1:n.*209del
XR_001738891.1:n.2747del
XR_939707.2:n.2747del
NM_022437.3:c.*209del MANE Select	NP_071882.1:n.*209del
NM_001357321.2:c.*209del	NP_001344250.1:n.*209del