Canonical Allele Identifier: CA2693446495

Gene: TSPAN7

Linked Data

• gnomAD v4: X-38675598-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675598T>C , CM000685.2:g.38675598T>C	GRCh38
NC_000023.10:g.38534852T>C , CM000685.1:g.38534852T>C	GRCh37
NC_000023.9:g.38419796T>C	NCBI36
NG_009160.1:g.119122T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.442-107T>C MANE Select	ENSP00000367743.2:n.442-107T>C
ENST00000286824.6:c.493-107T>C	ENSP00000286824.6:n.493-107T>C
ENST00000378482.6:c.442-107T>C	ENSP00000367743.2:n.442-107T>C
ENST00000419600.3:n.386-107T>C
ENST00000465127.1:c.532-107T>C	ENSP00000417050.1:n.532-107T>C
ENST00000471410.5:c.*468-107T>C	ENSP00000419290.1:n.*468-107T>C
ENST00000475216.5:c.*435-107T>C	ENSP00000418586.1:n.*435-107T>C
ENST00000488893.5:n.625-107T>C
NM_004615.3:c.442-107T>C	NP_004606.2:n.442-107T>C
NM_004615.4:c.442-107T>C MANE Select	NP_004606.2:n.442-107T>C