Canonical Allele Identifier: CA395643512

Gene: HSD3B7

Linked Data

• MyVariant Identifiers: chr16:g.30999286C>A (hg19) ; chr16:g.30987965C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30987965C>A , CM000678.2:g.30987965C>A	GRCh38
NC_000016.9:g.30999286C>A , CM000678.1:g.30999286C>A	GRCh37
NC_000016.8:g.30906787C>A	NCBI36
NG_012346.1:g.7768C>A
NG_041829.1:g.27544G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.892C>A MANE Select	ENSP00000297679.5:p.Leu298Met
ENST00000262520.10:c.*138C>A	ENSP00000262520.6:n.*138C>A
ENST00000297679.9:c.892C>A	ENSP00000297679.5:p.Leu298Met
NM_001142777.1:c.*138C>A	NP_001136249.1:n.*138C>A
NM_001142778.1:c.*138C>A	NP_001136250.1:n.*138C>A
NM_025193.3:c.892C>A	NP_079469.2:p.Leu298Met
XM_005255601.3:c.892C>A	XP_005255658.2:p.Leu298Met
XM_011545960.1:c.892C>A	XP_011544262.1:p.Leu298Met
XM_011545961.1:c.892C>A	XP_011544263.1:p.Leu298Met
XM_011545960.2:c.892C>A	XP_011544262.1:p.Leu298Met
XM_011545962.2:c.*138C>A	XP_011544264.1:n.*138C>A
XM_017023732.1:c.*138C>A	XP_016879221.1:n.*138C>A
NM_025193.4:c.892C>A MANE Select	NP_079469.2:p.Leu298Met
NM_001142777.2:c.*138C>A	NP_001136249.1:n.*138C>A
NM_001142778.2:c.*138C>A	NP_001136250.1:n.*138C>A