Canonical Allele Identifier: CA456684857

Gene: CYP3A5 ZSCAN25

Linked Data

• MyVariant Identifiers: chr7:g.99245934T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99648311T>G , CM000669.2:g.99648311T>G	GRCh38
NC_000007.13:g.99245934T>G , CM000669.1:g.99245934T>G	GRCh37
NC_000007.12:g.99083870T>G	NCBI36
NG_007938.1:g.36688A>C
NG_007938.2:g.36688A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000646887.1:c.*1188A>C (CYP3A5)	ENSP00000496704.1:n.*1188A>C
ENST00000222982.8:c.1503A>C (CYP3A5) MANE Select	ENSP00000222982.4:p.Gly501=
ENST00000339843.6:c.*2987A>C (CYP3A5)	ENSP00000343074.2:n.*2987A>C
ENST00000461920.5:n.2095A>C (CYP3A5)
ENST00000469887.5:n.3036A>C (CYP3A5)
NM_000777.4:c.1503A>C (CYP3A5)	NP_000768.1:p.Gly501=
NM_001291829.1:c.1164A>C (CYP3A5)	NP_001278758.1:p.Gly388=
NM_001291830.1:c.1473A>C (CYP3A5)	NP_001278759.1:p.Gly491=
NR_033807.2:n.3237A>C (CYP3A5)
XM_011515843.1:c.1164A>C (CYP3A5)	XP_011514145.1:p.Gly388=
XM_011515844.1:c.1164A>C (CYP3A5)	XP_011514146.1:p.Gly388=
XM_011515845.1:c.963A>C (CYP3A5)	XP_011514147.1:p.Gly321=
XM_011515846.1:c.963A>C (CYP3A5)	XP_011514148.1:p.Gly321=
XM_011515847.1:c.963A>C (CYP3A5)	XP_011514149.1:p.Gly321=
XM_011515909.1:c.806-20784T>G (ZSCAN25)	XP_011514211.1:n.806-20784T>G
XR_927402.1:n.1466+24131T>G (ZSCAN25)
NM_000777.5:c.1503A>C (CYP3A5) MANE Select	NP_000768.1:p.Gly501=
NM_001350984.1:c.806-20784T>G (ZSCAN25)	NP_001337913.1:n.806-20784T>G
NM_001350985.1:c.806-20784T>G (ZSCAN25)	NP_001337914.1:n.806-20784T>G
XM_011515909.2:c.806-20784T>G (ZSCAN25)	XP_011514211.1:n.806-20784T>G
XR_927402.2:n.1465+24131T>G (ZSCAN25)
NM_001291829.2:c.1164A>C (CYP3A5)	NP_001278758.1:p.Gly388=
NM_001291830.2:c.1473A>C (CYP3A5)	NP_001278759.1:p.Gly491=
NM_001350984.2:c.806-20784T>G (ZSCAN25)	NP_001337913.1:n.806-20784T>G
NM_001350985.2:c.806-20784T>G (ZSCAN25)	NP_001337914.1:n.806-20784T>G
NR_033807.3:n.3207A>C (CYP3A5)