Canonical Allele Identifier: CA2493961815

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43872104A= , CM000664.2:g.43872104A=	GRCh38
NC_000002.11:g.44099243A= , CM000664.1:g.44099243A=	GRCh37
NC_000002.10:g.43952747A=	NCBI36
NG_008884.1:g.38141A=
NG_008884.2:g.45163A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1093A= MANE Select	ENSP00000272286.2:p.Thr365=
ENST00000644611.1:c.1105A=	ENSP00000495423.1:p.Thr369=
ENST00000272286.2:c.1093A=	ENSP00000272286.2:p.Thr365=
NM_022437.2:c.1093A=	NP_071882.1:p.Thr365=
XM_005264483.2:c.1093A=	XP_005264540.1:p.Thr365=
XM_011533029.1:c.1105A=	XP_011531331.1:p.Thr369=
XM_011533030.1:c.1105A=	XP_011531332.1:p.Thr369=
XM_011533031.1:c.877A=	XP_011531333.1:p.Thr293=
XR_939707.1:n.1595A=
NM_001357321.1:c.1093A=	NP_001344250.1:p.Thr365=
XM_011533029.2:c.1105A=	XP_011531331.1:p.Thr369=
XM_011533030.2:c.1105A=	XP_011531332.1:p.Thr369=
XR_001738891.1:n.1609A=
XR_939707.2:n.1609A=
NM_022437.3:c.1093A= MANE Select	NP_071882.1:p.Thr365=
NM_001357321.2:c.1093A=	NP_001344250.1:p.Thr365=