Canonical Allele Identifier: CA10042755

Gene: TMPRSS3

Linked Data

• dbSNP Id: rs766067676
• ExAC: 21:43815411 G / A
• gnomAD v2: 21-43815411-G-A
• gnomAD v4: 21-42395302-G-A
• MyVariant Identifiers: chr21:g.43815411G>A (hg19) ; chr21:g.42395302G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42395302G>A , CM000683.2:g.42395302G>A	GRCh38
NC_000021.8:g.43815411G>A , CM000683.1:g.43815411G>A	GRCh37
NC_000021.7:g.42688480G>A	NCBI36
NG_011629.1:g.5790C>T
NG_011629.2:g.5790C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.94+22C>T	ENSP00000411013.3:n.94+22C>T
ENST00000644384.2:c.94+22C>T MANE Select	ENSP00000494414.1:n.94+22C>T
ENST00000652415.1:c.94+22C>T	ENSP00000498756.1:n.94+22C>T
ENST00000291532.7:c.94+22C>T	ENSP00000291532.3:n.94+22C>T
ENST00000398397.3:c.94+22C>T	ENSP00000381434.3:n.94+22C>T
ENST00000398405.5:c.94+22C>T	ENSP00000381442.1:n.94+22C>T
ENST00000433957.6:c.94+22C>T	ENSP00000411013.2:n.94+22C>T
NM_001256317.1:c.94+22C>T	NP_001243246.1:n.94+22C>T
NM_024022.2:c.94+22C>T	NP_076927.1:n.94+22C>T
NM_032405.1:c.94+22C>T	NP_115781.1:n.94+22C>T
NR_046020.1:n.1050+22C>T
NM_001256317.2:c.94+22C>T	NP_001243246.1:n.94+22C>T
NM_024022.3:c.94+22C>T	NP_076927.1:n.94+22C>T
NM_032405.2:c.94+22C>T	NP_115781.1:n.94+22C>T
NM_001256317.3:c.94+22C>T MANE Select	NP_001243246.1:n.94+22C>T
NM_024022.4:c.94+22C>T	NP_076927.1:n.94+22C>T