Canonical Allele Identifier: CA797724061

Gene: TMPRSS11A

Linked Data

• dbSNP Id: rs1198801829
• MyVariant Identifiers: chr4:g.68797786_68797788del (hg19) ; chr4:g.67932068_67932070del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67932072_67932074del , CM000666.2:g.67932072_67932074del	GRCh38
NC_000004.11:g.68797790_68797792del , CM000666.1:g.68797790_68797792del	GRCh37
NC_000004.10:g.68480385_68480387del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508048.6:c.253-10_253-8del MANE Select	ENSP00000426911.2:n.253-10_253-8del
ENST00000334830.11:c.262-10_262-8del	ENSP00000334611.7:n.262-10_262-8del
ENST00000396188.3:c.253-10_253-8del	ENSP00000379491.3:n.253-10_253-8del
ENST00000508048.5:c.253-10_253-8del	ENSP00000426911.2:n.253-10_253-8del
ENST00000513536.5:c.193-10_193-8del	ENSP00000427621.1:n.193-10_193-8del
NM_001114387.1:c.253-10_253-8del	NP_001107859.1:n.253-10_253-8del
NM_182606.3:c.262-10_262-8del	NP_872412.3:n.262-10_262-8del
NM_001114387.2:c.253-10_253-8del MANE Select	NP_001107859.1:n.253-10_253-8del
NM_182606.4:c.262-10_262-8del	NP_872412.3:n.262-10_262-8del