Canonical Allele Identifier: CA46426492

Gene: ABCG5 ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43838755G>A , CM000664.2:g.43838755G>A	GRCh38
NC_000002.11:g.44065894G>A , CM000664.1:g.44065894G>A	GRCh37
NC_000002.10:g.43919398G>A	NCBI36
NG_008883.1:g.5065C>T
NG_008884.1:g.4792G>A
NG_008884.2:g.11814G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022436.3:c.-76C>T (ABCG5) MANE Select	NP_071881.1:n.-76C>T
ENST00000405322.8:c.-76C>T (ABCG5) MANE Select	ENSP00000384513.2:n.-76C>T
NM_022436.2:c.-76C>T (ABCG5)	NP_071881.1:n.-76C>T
ENST00000260645.5:c.-76C>T (ABCG5)	ENSP00000260645.1:n.-76C>T
ENST00000409962.1:c.-900C>T (ABCG5)	ENSP00000386501.1:n.-900C>T
ENST00000643284.1:n.521-5752G>A (ABCG8)
ENST00000644611.1:c.76-5752G>A (ABCG8)	ENSP00000495423.1:n.76-5752G>A
XM_005264480.2:c.-76C>T (ABCG5)	XP_005264537.1:n.-76C>T
XM_005264480.4:c.-76C>T (ABCG5)	XP_005264537.1:n.-76C>T
XM_006712073.2:c.-76C>T (ABCG5)	XP_006712136.1:n.-76C>T
XM_006712073.3:c.-76C>T (ABCG5)	XP_006712136.1:n.-76C>T
XM_006712074.2:c.-76C>T (ABCG5)	XP_006712137.1:n.-76C>T
XM_006712074.3:c.-76C>T (ABCG5)	XP_006712137.1:n.-76C>T
XM_011533024.1:c.-76C>T (ABCG5)	XP_011531326.1:n.-76C>T
XM_011533024.2:c.-76C>T (ABCG5)	XP_011531326.1:n.-76C>T
XM_011533025.1:c.-819C>T (ABCG5)	XP_011531327.1:n.-819C>T
XM_011533025.3:c.-819C>T (ABCG5)	XP_011531327.1:n.-819C>T
XM_011533026.1:c.-76C>T (ABCG5)	XP_011531328.1:n.-76C>T
XM_011533026.2:c.-76C>T (ABCG5)	XP_011531328.1:n.-76C>T
XM_011533027.1:c.-934C>T (ABCG5)	XP_011531329.1:n.-934C>T
XM_011533027.3:c.-934C>T (ABCG5)	XP_011531329.1:n.-934C>T
XM_011533029.1:c.76-5752G>A (ABCG8)	XP_011531331.1:n.76-5752G>A
XM_011533029.2:c.76-5752G>A (ABCG8)	XP_011531331.1:n.76-5752G>A
XM_011533030.1:c.76-5752G>A (ABCG8)	XP_011531332.1:n.76-5752G>A
XM_011533030.2:c.76-5752G>A (ABCG8)	XP_011531332.1:n.76-5752G>A
XM_011533031.1:c.-153-5752G>A (ABCG8)	XP_011531333.1:n.-153-5752G>A
XR_001738891.1:n.580-5752G>A (ABCG8)
XR_939707.1:n.566-5752G>A (ABCG8)
XR_939707.2:n.580-5752G>A (ABCG8)