Canonical Allele Identifier: CA2658820920

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43839151-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43839154del , CM000664.2:g.43839154del	GRCh38
NC_000002.11:g.44066293del , CM000664.1:g.44066293del	GRCh37
NC_000002.10:g.43919797del	NCBI36
NG_008883.1:g.4668del
NG_008884.1:g.5191del
NG_008884.2:g.12213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.63+38del MANE Select	ENSP00000272286.2:n.63+38del
ENST00000643284.1:n.521-5353del
ENST00000644611.1:c.76-5353del	ENSP00000495423.1:n.76-5353del
ENST00000272286.2:c.63+38del	ENSP00000272286.2:n.63+38del
NM_022437.2:c.63+38del	NP_071882.1:n.63+38del
XM_005264483.2:c.63+38del	XP_005264540.1:n.63+38del
XM_011533029.1:c.76-5353del	XP_011531331.1:n.76-5353del
XM_011533030.1:c.76-5353del	XP_011531332.1:n.76-5353del
XM_011533031.1:c.-153-5353del	XP_011531333.1:n.-153-5353del
XR_939707.1:n.566-5353del
NM_001357321.1:c.63+38del	NP_001344250.1:n.63+38del
XM_011533029.2:c.76-5353del	XP_011531331.1:n.76-5353del
XM_011533030.2:c.76-5353del	XP_011531332.1:n.76-5353del
XR_001738891.1:n.580-5353del
XR_939707.2:n.580-5353del
NM_022437.3:c.63+38del MANE Select	NP_071882.1:n.63+38del
NM_001357321.2:c.63+38del	NP_001344250.1:n.63+38del