Canonical Allele Identifier: CA1729275128

Gene: CYP3A43

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99836455A= , CM000669.2:g.99836455A=	GRCh38
NC_000007.13:g.99434078A= , CM000669.1:g.99434078A=	GRCh37
NC_000007.12:g.99272014A=	NCBI36
NG_007935.1:g.13443A=

Transcript Alleles

HGVS	Amino-acid Change
NM_057095.3:c.74A= MANE Select	NP_476436.1:p.Tyr25=
ENST00000354829.7:c.74A= MANE Select	ENSP00000346887.3:p.Tyr25=
NM_001278921.1:c.74A=	NP_001265850.1:p.Tyr25=
NM_001278921.2:c.74A=	NP_001265850.1:p.Tyr25=
NM_022820.4:c.74A=	NP_073731.1:p.Tyr25=
NM_022820.5:c.74A=	NP_073731.1:p.Tyr25=
NM_057095.2:c.74A=	NP_476436.1:p.Tyr25=
NM_057096.3:c.74A=	NP_476437.1:p.Tyr25=
NM_057096.4:c.74A=	NP_476437.1:p.Tyr25=
NR_103868.1:n.175-2665A=
NR_103868.2:n.175-2665A=
NR_103869.1:n.177A=
NR_103869.2:n.177A=
ENST00000222382.5:c.74A=	ENSP00000222382.5:p.Tyr25=
ENST00000312017.9:c.74A=	ENSP00000312110.5:p.Tyr25=
ENST00000342499.8:c.74A=	ENSP00000345351.5:p.Tyr25=
ENST00000354829.6:c.74A=	ENSP00000346887.2:p.Tyr25=
ENST00000415413.5:c.74A=	ENSP00000401521.1:p.Tyr25=
ENST00000417625.5:c.74A=	ENSP00000416581.1:p.Tyr25=
ENST00000433277.5:c.74A=	ENSP00000400316.1:p.Tyr25=
ENST00000434806.5:c.74A=	ENSP00000411653.1:p.Tyr25=
ENST00000436834.5:c.72-2665A=	ENSP00000415221.1:n.72-2665A=
ENST00000444905.5:c.39+8269A=	ENSP00000405557.1:n.39+8269A=
ENST00000463915.5:n.138+8269A=
ENST00000477658.5:n.138+8269A=
ENST00000481362.5:n.74A=
ENST00000491648.5:n.138+8269A=
ENST00000495115.5:n.138+8269A=
ENST00000631161.2:c.74A=	ENSP00000486759.1:p.Tyr25=
XM_011516493.1:c.74A=	XP_011514795.1:p.Tyr25=
XM_024446877.1:c.-157A=	XP_024302645.1:n.-157A=