Canonical Allele Identifier: CA2544847159

Gene: TSPAN7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38676014G>T , CM000685.2:g.38676014G>T	GRCh38
NC_000023.10:g.38535268G>T , CM000685.1:g.38535268G>T	GRCh37
NC_000023.9:g.38420212G>T	NCBI36
NG_009160.1:g.119538G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+154G>T MANE Select	ENSP00000367743.2:n.597+154G>T
ENST00000286824.6:c.648+154G>T	ENSP00000286824.6:n.648+154G>T
ENST00000378482.6:c.597+154G>T	ENSP00000367743.2:n.597+154G>T
ENST00000419600.3:n.541+154G>T
ENST00000465127.1:c.687+154G>T	ENSP00000417050.1:n.687+154G>T
ENST00000471410.5:c.*623+154G>T	ENSP00000419290.1:n.*623+154G>T
ENST00000475216.5:c.*590+154G>T	ENSP00000418586.1:n.*590+154G>T
NM_004615.3:c.597+154G>T	NP_004606.2:n.597+154G>T
NM_004615.4:c.597+154G>T MANE Select	NP_004606.2:n.597+154G>T