Canonical Allele Identifier: CA2616036348

Gene: TMPRSS5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113690156C>T , CM000673.2:g.113690156C>T	GRCh38
NC_000011.9:g.113560878C>T , CM000673.1:g.113560878C>T	GRCh37
NC_000011.8:g.113066088C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_030770.4:c.1206+75G>A MANE Select	NP_110397.2:n.1206+75G>A
ENST00000299882.11:c.1206+75G>A MANE Select	ENSP00000299882.5:n.1206+75G>A
NM_001288749.1:c.867+75G>A	NP_001275678.1:n.867+75G>A
NM_001288749.2:c.867+75G>A	NP_001275678.1:n.867+75G>A
NM_001288750.1:c.1074+75G>A	NP_001275679.1:n.1074+75G>A
NM_001288750.2:c.1074+75G>A	NP_001275679.1:n.1074+75G>A
NM_001288751.1:c.1179+75G>A	NP_001275680.1:n.1179+75G>A
NM_001288751.2:c.1179+75G>A	NP_001275680.1:n.1179+75G>A
NM_001288752.1:c.999+75G>A	NP_001275681.1:n.999+75G>A
NM_001288752.2:c.999+75G>A	NP_001275681.1:n.999+75G>A
NM_030770.3:c.1206+75G>A	NP_110397.2:n.1206+75G>A
NR_110046.1:n.1153+75G>A
NR_110046.2:n.1088+75G>A
NR_110047.1:n.1153+75G>A
NR_110047.2:n.1088+75G>A
ENST00000299882.9:c.1206+75G>A	ENSP00000299882.5:n.1206+75G>A
ENST00000536856.5:c.429+75G>A	ENSP00000437937.1:n.429+75G>A
ENST00000538955.5:c.1074+75G>A	ENSP00000445528.1:n.1074+75G>A
ENST00000540540.5:c.429+75G>A	ENSP00000437761.1:n.429+75G>A
ENST00000544476.1:c.867+75G>A	ENSP00000445930.1:n.867+75G>A
ENST00000544634.5:c.999+75G>A	ENSP00000440783.1:n.999+75G>A
ENST00000545579.5:c.1179+75G>A	ENSP00000441104.1:n.1179+75G>A
ENST00000545579.6:c.1179+75G>A	ENSP00000441104.1:n.1179+75G>A
ENST00000645981.1:c.*1175+75G>A	ENSP00000496410.1:n.*1175+75G>A
XM_011543014.1:c.1197+75G>A	XP_011541316.1:n.1197+75G>A
XM_011543015.1:c.1206+75G>A	XP_011541317.1:n.1206+75G>A
XM_017018366.1:c.516+75G>A	XP_016873855.1:n.516+75G>A
XM_017018367.1:c.516+75G>A	XP_016873856.1:n.516+75G>A
XR_001747990.1:n.6021+75G>A
XR_001747991.1:n.6125+75G>A
XR_001747992.1:n.5918+75G>A