Canonical Allele Identifier: CA2976610063

Gene: TMPRSS5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113690163dup , CM000673.2:g.113690163dup	GRCh38
NC_000011.9:g.113560885dup , CM000673.1:g.113560885dup	GRCh37
NC_000011.8:g.113066095dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_030770.4:c.1206+68dup MANE Select	NP_110397.2:n.1206+68dup
ENST00000299882.11:c.1206+68dup MANE Select	ENSP00000299882.5:n.1206+68dup
NM_001288749.1:c.867+68dup	NP_001275678.1:n.867+68dup
NM_001288749.2:c.867+68dup	NP_001275678.1:n.867+68dup
NM_001288750.1:c.1074+68dup	NP_001275679.1:n.1074+68dup
NM_001288750.2:c.1074+68dup	NP_001275679.1:n.1074+68dup
NM_001288751.1:c.1179+68dup	NP_001275680.1:n.1179+68dup
NM_001288751.2:c.1179+68dup	NP_001275680.1:n.1179+68dup
NM_001288752.1:c.999+68dup	NP_001275681.1:n.999+68dup
NM_001288752.2:c.999+68dup	NP_001275681.1:n.999+68dup
NM_030770.3:c.1206+68dup	NP_110397.2:n.1206+68dup
NR_110046.1:n.1153+68dup
NR_110046.2:n.1088+68dup
NR_110047.1:n.1153+68dup
NR_110047.2:n.1088+68dup
ENST00000299882.9:c.1206+68dup	ENSP00000299882.5:n.1206+68dup
ENST00000536856.5:c.429+68dup	ENSP00000437937.1:n.429+68dup
ENST00000538955.5:c.1074+68dup	ENSP00000445528.1:n.1074+68dup
ENST00000540540.5:c.429+68dup	ENSP00000437761.1:n.429+68dup
ENST00000544476.1:c.867+68dup	ENSP00000445930.1:n.867+68dup
ENST00000544634.5:c.999+68dup	ENSP00000440783.1:n.999+68dup
ENST00000545579.5:c.1179+68dup	ENSP00000441104.1:n.1179+68dup
ENST00000545579.6:c.1179+68dup	ENSP00000441104.1:n.1179+68dup
ENST00000645981.1:c.*1175+68dup	ENSP00000496410.1:n.*1175+68dup
XM_011543014.1:c.1197+68dup	XP_011541316.1:n.1197+68dup
XM_011543015.1:c.1206+68dup	XP_011541317.1:n.1206+68dup
XM_017018366.1:c.516+68dup	XP_016873855.1:n.516+68dup
XM_017018367.1:c.516+68dup	XP_016873856.1:n.516+68dup
XR_001747990.1:n.6021+68dup
XR_001747991.1:n.6125+68dup
XR_001747992.1:n.5918+68dup