Canonical Allele Identifier: CA1459044867
Gene: SRD5A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346334G= , CM000666.2:g.55346334G= GRCh38
NC_000004.11:g.56212501G= , CM000666.1:g.56212501G= GRCh37
NC_000004.10:g.55907258G= NCBI36
NG_028230.1:g.5114G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.-3G= MANE Select ENSP00000264228.4:n.-3G=
ENST00000679351.1:c.-3G= ENSP00000505676.1:n.-3G=
ENST00000679707.1:c.-3G= ENSP00000505713.1:n.-3G=
ENST00000679836.1:c.-3G= ENSP00000506601.1:n.-3G=
ENST00000680700.1:c.-3G= ENSP00000504926.1:n.-3G=
ENST00000264228.8:c.-3G= ENSP00000264228.4:n.-3G=
NM_024592.4:c.-3G= NP_078868.1:n.-3G=
XM_005265766.2:c.-3G= XP_005265823.1:n.-3G=
XM_005265767.2:c.-3G= XP_005265824.1:n.-3G=
XM_005265766.4:c.-3G= XP_005265823.1:n.-3G=
XM_005265767.3:c.-3G= XP_005265824.1:n.-3G=
NM_024592.5:c.-3G= MANE Select NP_078868.1:n.-3G=