Canonical Allele Identifier: CA2820495039

Gene: TSPAN7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38676003G>C , CM000685.2:g.38676003G>C	GRCh38
NC_000023.10:g.38535257G>C , CM000685.1:g.38535257G>C	GRCh37
NC_000023.9:g.38420201G>C	NCBI36
NG_009160.1:g.119527G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+143G>C MANE Select	ENSP00000367743.2:n.597+143G>C
ENST00000286824.6:c.648+143G>C	ENSP00000286824.6:n.648+143G>C
ENST00000378482.6:c.597+143G>C	ENSP00000367743.2:n.597+143G>C
ENST00000419600.3:n.541+143G>C
ENST00000465127.1:c.687+143G>C	ENSP00000417050.1:n.687+143G>C
ENST00000471410.5:c.*623+143G>C	ENSP00000419290.1:n.*623+143G>C
ENST00000475216.5:c.*590+143G>C	ENSP00000418586.1:n.*590+143G>C
NM_004615.3:c.597+143G>C	NP_004606.2:n.597+143G>C
NM_004615.4:c.597+143G>C MANE Select	NP_004606.2:n.597+143G>C