Canonical Allele Identifier: CA410369055

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42375869C>G , CM000683.2:g.42375869C>G	GRCh38
NC_000021.8:g.43795978C>G , CM000683.1:g.43795978C>G	GRCh37
NC_000021.7:g.42669047C>G	NCBI36
NG_011629.1:g.25223G>C
NG_011629.2:g.25223G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001256317.3:c.1192-1G>C MANE Select	NP_001243246.1:n.1192-1G>C
ENST00000644384.2:c.1192-1G>C MANE Select	ENSP00000494414.1:n.1192-1G>C
NM_001256317.1:c.1192-1G>C	NP_001243246.1:n.1192-1G>C
NM_001256317.2:c.1192-1G>C	NP_001243246.1:n.1192-1G>C
NM_024022.2:c.1195-1G>C	NP_076927.1:n.1195-1G>C
NM_024022.3:c.1195-1G>C	NP_076927.1:n.1195-1G>C
NM_024022.4:c.1195-1G>C	NP_076927.1:n.1195-1G>C
NM_032404.2:c.814-1G>C	NP_115780.1:n.814-1G>C
NM_032404.3:c.814-1G>C	NP_115780.1:n.814-1G>C
NR_046020.1:n.2151-1G>C
ENST00000291532.7:c.1195-1G>C	ENSP00000291532.3:n.1195-1G>C
ENST00000398405.5:c.1186-1G>C	ENSP00000381442.1:n.1186-1G>C
ENST00000433957.6:c.1192-1G>C	ENSP00000411013.2:n.1192-1G>C
ENST00000433957.7:c.1195-1G>C	ENSP00000411013.3:n.1195-1G>C
ENST00000474596.5:n.1063-1G>C
ENST00000476848.5:n.1927-1G>C
ENST00000482761.1:n.1482-1G>C
ENST00000652415.1:c.1192-1G>C	ENSP00000498756.1:n.1192-1G>C