Canonical Allele Identifier: CA409847916

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653397G>C (hg19) ; chr21:g.18281080G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281080G>C , CM000683.2:g.18281080G>C	GRCh38
NC_000021.8:g.19653397G>C , CM000683.1:g.19653397G>C	GRCh37
NC_000021.7:g.18575268G>C	NCBI36
NG_012207.1:g.127574C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2628C>G MANE Select	ENSP00000284885.3:p.Asp876Glu
ENST00000284885.7:c.2628C>G	ENSP00000284885.3:p.Asp876Glu
NM_002772.2:c.2628C>G	NP_002763.2:p.Asp876Glu
XM_011529654.1:c.2763C>G	XP_011527956.1:p.Asp921Glu
XM_011529655.1:c.2763C>G	XP_011527957.1:p.Asp921Glu
XM_011529656.1:c.2763C>G	XP_011527958.1:p.Asp921Glu
XM_011529657.1:c.2718C>G	XP_011527959.1:p.Asp906Glu
XM_011529658.1:c.2682C>G	XP_011527960.1:p.Asp894Glu
XM_011529659.1:c.2673C>G	XP_011527961.1:p.Asp891Glu
XM_011529654.2:c.2763C>G	XP_011527956.1:p.Asp921Glu
XM_011529656.2:c.2763C>G	XP_011527958.1:p.Asp921Glu
XM_011529657.2:c.2718C>G	XP_011527959.1:p.Asp906Glu
XM_011529658.2:c.2682C>G	XP_011527960.1:p.Asp894Glu
NM_002772.3:c.2628C>G MANE Select	NP_002763.3:p.Asp876Glu