Canonical Allele Identifier: CA2925206
Community Standard Title: NM_024592.5(SRD5A3):c.108G>T (p.Pro36=)
Gene: SRD5A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346444G>T , CM000666.2:g.55346444G>T GRCh38
NC_000004.11:g.56212611G>T , CM000666.1:g.56212611G>T GRCh37
NC_000004.10:g.55907368G>T NCBI36
NG_028230.1:g.5224G>T

Transcript Alleles

HGVS Amino-acid Change
NM_024592.5:c.108G>T MANE Select NP_078868.1:p.Pro36=
ENST00000264228.9:c.108G>T MANE Select ENSP00000264228.4:p.Pro36=
NM_024592.4:c.108G>T NP_078868.1:p.Pro36=
ENST00000264228.8:c.108G>T ENSP00000264228.4:p.Pro36=
ENST00000505210.1:c.33G>T ENSP00000424714.1:p.Pro11=
ENST00000679351.1:c.108G>T ENSP00000505676.1:p.Pro36=
ENST00000679707.1:c.108G>T ENSP00000505713.1:p.Pro36=
ENST00000679836.1:c.108G>T ENSP00000506601.1:p.Pro36=
ENST00000680700.1:c.108G>T ENSP00000504926.1:p.Pro36=
XM_005265766.2:c.108G>T XP_005265823.1:p.Pro36=
XM_005265766.4:c.108G>T XP_005265823.1:p.Pro36=
XM_005265767.2:c.108G>T XP_005265824.1:p.Pro36=
XM_005265767.3:c.108G>T XP_005265824.1:p.Pro36=