Canonical Allele Identifier: CA456688798

Gene: CYP3A5 ZSCAN25

Linked Data

• MyVariant Identifiers: chr7:g.99262886C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99665263C>G , CM000669.2:g.99665263C>G	GRCh38
NC_000007.13:g.99262886C>G , CM000669.1:g.99262886C>G	GRCh37
NC_000007.12:g.99100822C>G	NCBI36
NG_007938.1:g.19736G>C
NG_007938.2:g.19736G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646887.1:c.*258G>C (CYP3A5)	ENSP00000496704.1:n.*258G>C
ENST00000222982.8:c.573G>C (CYP3A5) MANE Select	ENSP00000222982.4:p.Val191=
ENST00000339843.6:c.*972G>C (CYP3A5)	ENSP00000343074.2:n.*972G>C
ENST00000461920.5:n.1165G>C (CYP3A5)
ENST00000463364.5:n.892G>C (CYP3A5)
ENST00000466061.5:n.913G>C (CYP3A5)
ENST00000469887.5:n.1021G>C (CYP3A5)
ENST00000481825.5:n.1173G>C (CYP3A5)
NM_000777.4:c.573G>C (CYP3A5)	NP_000768.1:p.Val191=
NM_001291829.1:c.234G>C (CYP3A5)	NP_001278758.1:p.Val78=
NM_001291830.1:c.543G>C (CYP3A5)	NP_001278759.1:p.Val181=
NR_033807.2:n.1222G>C (CYP3A5)
XM_006715859.2:c.573G>C (CYP3A5)	XP_006715922.1:p.Val191=
XM_011515843.1:c.234G>C (CYP3A5)	XP_011514145.1:p.Val78=
XM_011515844.1:c.234G>C (CYP3A5)	XP_011514146.1:p.Val78=
XM_011515845.1:c.33G>C (CYP3A5)	XP_011514147.1:p.Val11=
XM_011515846.1:c.33G>C (CYP3A5)	XP_011514148.1:p.Val11=
XM_011515847.1:c.33G>C (CYP3A5)	XP_011514149.1:p.Val11=
XM_011515909.1:c.806-3832C>G (ZSCAN25)	XP_011514211.1:n.806-3832C>G
XR_927402.1:n.1466+41083C>G (ZSCAN25)
NM_000777.5:c.573G>C (CYP3A5) MANE Select	NP_000768.1:p.Val191=
NM_001350984.1:c.806-3832C>G (ZSCAN25)	NP_001337913.1:n.806-3832C>G
NM_001350985.1:c.806-3832C>G (ZSCAN25)	NP_001337914.1:n.806-3832C>G
XM_011515909.2:c.806-3832C>G (ZSCAN25)	XP_011514211.1:n.806-3832C>G
XR_927402.2:n.1465+41083C>G (ZSCAN25)
NM_001291829.2:c.234G>C (CYP3A5)	NP_001278758.1:p.Val78=
NM_001291830.2:c.543G>C (CYP3A5)	NP_001278759.1:p.Val181=
NM_001350984.2:c.806-3832C>G (ZSCAN25)	NP_001337913.1:n.806-3832C>G
NM_001350985.2:c.806-3832C>G (ZSCAN25)	NP_001337914.1:n.806-3832C>G
NR_033807.3:n.1192G>C (CYP3A5)