Canonical Allele Identifier: CA2216820866

Gene: HSD3B7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30986064_30986066delinsCTG , CM000678.2:g.30986064_30986066delinsCTG	GRCh38
NC_000016.9:g.30997385_30997387delinsCTG , CM000678.1:g.30997385_30997387delinsCTG	GRCh37
NC_000016.8:g.30904886_30904888delinsCTG	NCBI36
NG_012346.1:g.5867_5869delinsCTG
NG_052948.1:g.33771_33773delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.182_184delinsCTG MANE Select	ENSP00000297679.5:p.Thr61=
ENST00000262520.10:c.182_184delinsCTG	ENSP00000262520.6:p.Thr61=
ENST00000297679.9:c.182_184delinsCTG	ENSP00000297679.5:p.Thr61=
ENST00000562932.5:c.305_307delinsCTG	ENSP00000459852.1:p.Thr102=
ENST00000574447.1:c.182_184delinsCTG	ENSP00000459689.1:p.Thr61=
NM_001142777.1:c.182_184delinsCTG	NP_001136249.1:p.Thr61=
NM_001142778.1:c.182_184delinsCTG	NP_001136250.1:p.Thr61=
NM_025193.3:c.182_184delinsCTG	NP_079469.2:p.Thr61=
XM_005255601.3:c.182_184delinsCTG	XP_005255658.2:p.Thr61=
XM_011545960.1:c.182_184delinsCTG	XP_011544262.1:p.Thr61=
XM_011545961.1:c.182_184delinsCTG	XP_011544263.1:p.Thr61=
XM_011545962.1:c.182_184delinsCTG	XP_011544264.1:p.Thr61=
XM_011545960.2:c.182_184delinsCTG	XP_011544262.1:p.Thr61=
XM_011545962.2:c.182_184delinsCTG	XP_011544264.1:p.Thr61=
XM_017023732.1:c.182_184delinsCTG	XP_016879221.1:p.Thr61=
NM_025193.4:c.182_184delinsCTG MANE Select	NP_079469.2:p.Thr61=
NM_001142777.2:c.182_184delinsCTG	NP_001136249.1:p.Thr61=
NM_001142778.2:c.182_184delinsCTG	NP_001136250.1:p.Thr61=