Canonical Allele Identifier: CA368365516
Gene: CYP3A5 HGNC NCBI
ZSCAN25 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99665217T>C , CM000669.2:g.99665217T>C GRCh38
NC_000007.13:g.99262840T>C , CM000669.1:g.99262840T>C GRCh37
NC_000007.12:g.99100776T>C NCBI36
NG_007938.1:g.19782A>G
NG_007938.2:g.19782A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646887.1:c.*304A>G (CYP3A5) ENSP00000496704.1:n.*304A>G
ENST00000222982.8:c.619A>G (CYP3A5) MANE Select ENSP00000222982.4:p.Thr207Ala
ENST00000339843.6:c.*1018A>G (CYP3A5) ENSP00000343074.2:n.*1018A>G
ENST00000461920.5:n.1211A>G (CYP3A5)
ENST00000463364.5:n.938A>G (CYP3A5)
ENST00000466061.5:n.959A>G (CYP3A5)
ENST00000469887.5:n.1067A>G (CYP3A5)
ENST00000481825.5:n.1219A>G (CYP3A5)
NM_000777.4:c.619A>G (CYP3A5) NP_000768.1:p.Thr207Ala
NM_001291829.1:c.280A>G (CYP3A5) NP_001278758.1:p.Thr94Ala
NM_001291830.1:c.589A>G (CYP3A5) NP_001278759.1:p.Thr197Ala
NR_033807.2:n.1268A>G (CYP3A5)
XM_006715859.2:c.619A>G (CYP3A5) XP_006715922.1:p.Thr207Ala
XM_011515843.1:c.280A>G (CYP3A5) XP_011514145.1:p.Thr94Ala
XM_011515844.1:c.280A>G (CYP3A5) XP_011514146.1:p.Thr94Ala
XM_011515845.1:c.79A>G (CYP3A5) XP_011514147.1:p.Thr27Ala
XM_011515846.1:c.79A>G (CYP3A5) XP_011514148.1:p.Thr27Ala
XM_011515847.1:c.79A>G (CYP3A5) XP_011514149.1:p.Thr27Ala
XM_011515909.1:c.806-3878T>C (ZSCAN25) XP_011514211.1:n.806-3878T>C
XR_927402.1:n.1466+41037T>C (ZSCAN25)
NM_000777.5:c.619A>G (CYP3A5) MANE Select NP_000768.1:p.Thr207Ala
NM_001350984.1:c.806-3878T>C (ZSCAN25) NP_001337913.1:n.806-3878T>C
NM_001350985.1:c.806-3878T>C (ZSCAN25) NP_001337914.1:n.806-3878T>C
XM_011515909.2:c.806-3878T>C (ZSCAN25) XP_011514211.1:n.806-3878T>C
XR_927402.2:n.1465+41037T>C (ZSCAN25)
NM_001291829.2:c.280A>G (CYP3A5) NP_001278758.1:p.Thr94Ala
NM_001291830.2:c.589A>G (CYP3A5) NP_001278759.1:p.Thr197Ala
NM_001350984.2:c.806-3878T>C (ZSCAN25) NP_001337913.1:n.806-3878T>C
NM_001350985.2:c.806-3878T>C (ZSCAN25) NP_001337914.1:n.806-3878T>C
NR_033807.3:n.1238A>G (CYP3A5)