Canonical Allele Identifier: CA2424970059

Gene: TSPAN7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675808A= , CM000685.2:g.38675808A=	GRCh38
NC_000023.10:g.38535062A= , CM000685.1:g.38535062A=	GRCh37
NC_000023.9:g.38420006A=	NCBI36
NG_009160.1:g.119332A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.545A= MANE Select	ENSP00000367743.2:p.Asn182=
ENST00000286824.6:c.596A=	ENSP00000286824.6:p.Asn199=
ENST00000378482.6:c.545A=	ENSP00000367743.2:p.Asn182=
ENST00000419600.3:n.489A=
ENST00000465127.1:c.635A=	ENSP00000417050.1:p.Asn212=
ENST00000471410.5:c.*571A=	ENSP00000419290.1:n.*571A=
ENST00000475216.5:c.*538A=	ENSP00000418586.1:n.*538A=
ENST00000488893.5:n.728A=
NM_004615.3:c.545A=	NP_004606.2:p.Asn182=
NM_004615.4:c.545A= MANE Select	NP_004606.2:p.Asn182=