Canonical Allele Identifier: CA395643198

Gene: HSD3B7

Linked Data

• COSMIC: COSM6144365
• MyVariant Identifiers: chr16:g.30999232G>T (hg19) ; chr16:g.30987911G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30987911G>T , CM000678.2:g.30987911G>T	GRCh38
NC_000016.9:g.30999232G>T , CM000678.1:g.30999232G>T	GRCh37
NC_000016.8:g.30906733G>T	NCBI36
NG_012346.1:g.7714G>T
NG_041829.1:g.27598C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.838G>T MANE Select	ENSP00000297679.5:p.Gly280Ter
ENST00000262520.10:c.*84G>T	ENSP00000262520.6:n.*84G>T
ENST00000297679.9:c.838G>T	ENSP00000297679.5:p.Gly280Ter
NM_001142777.1:c.*84G>T	NP_001136249.1:n.*84G>T
NM_001142778.1:c.*84G>T	NP_001136250.1:n.*84G>T
NM_025193.3:c.838G>T	NP_079469.2:p.Gly280Ter
XM_005255601.3:c.838G>T	XP_005255658.2:p.Gly280Ter
XM_011545960.1:c.838G>T	XP_011544262.1:p.Gly280Ter
XM_011545961.1:c.838G>T	XP_011544263.1:p.Gly280Ter
XM_011545962.1:c.*84G>T	XP_011544264.1:n.*84G>T
XM_011545960.2:c.838G>T	XP_011544262.1:p.Gly280Ter
XM_011545962.2:c.*84G>T	XP_011544264.1:n.*84G>T
XM_017023732.1:c.*84G>T	XP_016879221.1:n.*84G>T
NM_025193.4:c.838G>T MANE Select	NP_079469.2:p.Gly280Ter
NM_001142777.2:c.*84G>T	NP_001136249.1:n.*84G>T
NM_001142778.2:c.*84G>T	NP_001136250.1:n.*84G>T