Canonical Allele Identifier: CA2216820883

Gene: HSD3B7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30986073_30986074delinsAG , CM000678.2:g.30986073_30986074delinsAG	GRCh38
NC_000016.9:g.30997394_30997395delinsAG , CM000678.1:g.30997394_30997395delinsAG	GRCh37
NC_000016.8:g.30904895_30904896delinsAG	NCBI36
NG_012346.1:g.5876_5877delinsAG
NG_052948.1:g.33780_33781delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.191_192delinsAG MANE Select	ENSP00000297679.5:p.Gln64=
ENST00000262520.10:c.191_192delinsAG	ENSP00000262520.6:p.Gln64=
ENST00000297679.9:c.191_192delinsAG	ENSP00000297679.5:p.Gln64=
ENST00000562932.5:c.314_315delinsAG	ENSP00000459852.1:p.Gln105=
ENST00000574447.1:c.191_192delinsAG	ENSP00000459689.1:p.Gln64=
NM_001142777.1:c.191_192delinsAG	NP_001136249.1:p.Gln64=
NM_001142778.1:c.191_192delinsAG	NP_001136250.1:p.Gln64=
NM_025193.3:c.191_192delinsAG	NP_079469.2:p.Gln64=
XM_005255601.3:c.191_192delinsAG	XP_005255658.2:p.Gln64=
XM_011545960.1:c.191_192delinsAG	XP_011544262.1:p.Gln64=
XM_011545961.1:c.191_192delinsAG	XP_011544263.1:p.Gln64=
XM_011545962.1:c.191_192delinsAG	XP_011544264.1:p.Gln64=
XM_011545960.2:c.191_192delinsAG	XP_011544262.1:p.Gln64=
XM_011545962.2:c.191_192delinsAG	XP_011544264.1:p.Gln64=
XM_017023732.1:c.191_192delinsAG	XP_016879221.1:p.Gln64=
NM_025193.4:c.191_192delinsAG MANE Select	NP_079469.2:p.Gln64=
NM_001142777.2:c.191_192delinsAG	NP_001136249.1:p.Gln64=
NM_001142778.2:c.191_192delinsAG	NP_001136250.1:p.Gln64=