Canonical Allele Identifier: CA2216822088

Gene: HSD3B7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30986556_30986560delinsCTAAG , CM000678.2:g.30986556_30986560delinsCTAAG	GRCh38
NC_000016.9:g.30997877_30997881delinsCTAAG , CM000678.1:g.30997877_30997881delinsCTAAG	GRCh37
NC_000016.8:g.30905378_30905382delinsCTAAG	NCBI36
NG_012346.1:g.6359_6363delinsCTAAG
NG_052948.1:g.34263_34267delinsCTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.431+25_431+29delinsCTAAG MANE Select	ENSP00000297679.5:n.431+25_431+29delinsCTAAG
ENST00000262520.10:c.431+25_431+29delinsCTAAG	ENSP00000262520.6:n.431+25_431+29delinsCTAAG
ENST00000297679.9:c.431+25_431+29delinsCTAAG	ENSP00000297679.5:n.431+25_431+29delinsCTAAG
ENST00000562932.5:c.554+25_554+29delinsCTAAG	ENSP00000459852.1:n.554+25_554+29delinsCTAAG
ENST00000574447.1:c.431+25_431+29delinsCTAAG	ENSP00000459689.1:n.431+25_431+29delinsCTAAG
NM_001142777.1:c.431+25_431+29delinsCTAAG	NP_001136249.1:n.431+25_431+29delinsCTAAG
NM_001142778.1:c.431+25_431+29delinsCTAAG	NP_001136250.1:n.431+25_431+29delinsCTAAG
NM_025193.3:c.431+25_431+29delinsCTAAG	NP_079469.2:n.431+25_431+29delinsCTAAG
XM_005255601.3:c.431+25_431+29delinsCTAAG	XP_005255658.2:n.431+25_431+29delinsCTAAG
XM_011545960.1:c.431+25_431+29delinsCTAAG	XP_011544262.1:n.431+25_431+29delinsCTAAG
XM_011545961.1:c.431+25_431+29delinsCTAAG	XP_011544263.1:n.431+25_431+29delinsCTAAG
XM_011545962.1:c.431+25_431+29delinsCTAAG	XP_011544264.1:n.431+25_431+29delinsCTAAG
XM_011545960.2:c.431+25_431+29delinsCTAAG	XP_011544262.1:n.431+25_431+29delinsCTAAG
XM_011545962.2:c.431+25_431+29delinsCTAAG	XP_011544264.1:n.431+25_431+29delinsCTAAG
XM_017023732.1:c.431+25_431+29delinsCTAAG	XP_016879221.1:n.431+25_431+29delinsCTAAG
NM_025193.4:c.431+25_431+29delinsCTAAG MANE Select	NP_079469.2:n.431+25_431+29delinsCTAAG
NM_001142777.2:c.431+25_431+29delinsCTAAG	NP_001136249.1:n.431+25_431+29delinsCTAAG
NM_001142778.2:c.431+25_431+29delinsCTAAG	NP_001136250.1:n.431+25_431+29delinsCTAAG