Canonical Allele Identifier: CA409848068

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653468G>C (hg19) ; chr21:g.18281151G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281151G>C , CM000683.2:g.18281151G>C	GRCh38
NC_000021.8:g.19653468G>C , CM000683.1:g.19653468G>C	GRCh37
NC_000021.7:g.18575339G>C	NCBI36
NG_012207.1:g.127503C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2557C>G MANE Select	ENSP00000284885.3:p.Gln853Glu
ENST00000284885.7:c.2557C>G	ENSP00000284885.3:p.Gln853Glu
NM_002772.2:c.2557C>G	NP_002763.2:p.Gln853Glu
XM_011529654.1:c.2692C>G	XP_011527956.1:p.Gln898Glu
XM_011529655.1:c.2692C>G	XP_011527957.1:p.Gln898Glu
XM_011529656.1:c.2692C>G	XP_011527958.1:p.Gln898Glu
XM_011529657.1:c.2647C>G	XP_011527959.1:p.Gln883Glu
XM_011529658.1:c.2611C>G	XP_011527960.1:p.Gln871Glu
XM_011529659.1:c.2602C>G	XP_011527961.1:p.Gln868Glu
XM_011529654.2:c.2692C>G	XP_011527956.1:p.Gln898Glu
XM_011529656.2:c.2692C>G	XP_011527958.1:p.Gln898Glu
XM_011529657.2:c.2647C>G	XP_011527959.1:p.Gln883Glu
XM_011529658.2:c.2611C>G	XP_011527960.1:p.Gln871Glu
NM_002772.3:c.2557C>G MANE Select	NP_002763.3:p.Gln853Glu