Canonical Allele Identifier: CA2216823032

Gene: HSD3B7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30986921T= , CM000678.2:g.30986921T=	GRCh38
NC_000016.9:g.30998242T= , CM000678.1:g.30998242T=	GRCh37
NC_000016.8:g.30905743T=	NCBI36
NG_012346.1:g.6724T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.613T= MANE Select	ENSP00000297679.5:p.Phe205=
ENST00000262520.10:c.531+217T=	ENSP00000262520.6:n.531+217T=
ENST00000297679.9:c.613T=	ENSP00000297679.5:p.Phe205=
NM_001142777.1:c.531+217T=	NP_001136249.1:n.531+217T=
NM_001142778.1:c.531+217T=	NP_001136250.1:n.531+217T=
NM_025193.3:c.613T=	NP_079469.2:p.Phe205=
XM_005255601.3:c.613T=	XP_005255658.2:p.Phe205=
XM_011545960.1:c.613T=	XP_011544262.1:p.Phe205=
XM_011545961.1:c.613T=	XP_011544263.1:p.Phe205=
XM_011545962.1:c.531+217T=	XP_011544264.1:n.531+217T=
XM_011545960.2:c.613T=	XP_011544262.1:p.Phe205=
XM_011545962.2:c.531+217T=	XP_011544264.1:n.531+217T=
XM_017023732.1:c.531+217T=	XP_016879221.1:n.531+217T=
NM_025193.4:c.613T= MANE Select	NP_079469.2:p.Phe205=
NM_001142777.2:c.531+217T=	NP_001136249.1:n.531+217T=
NM_001142778.2:c.531+217T=	NP_001136250.1:n.531+217T=