Canonical Allele Identifier: CA2693446525

Gene: TSPAN7

Linked Data

• gnomAD v4: X-38675883-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675883G>C , CM000685.2:g.38675883G>C	GRCh38
NC_000023.10:g.38535137G>C , CM000685.1:g.38535137G>C	GRCh37
NC_000023.9:g.38420081G>C	NCBI36
NG_009160.1:g.119407G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+23G>C MANE Select	ENSP00000367743.2:n.597+23G>C
ENST00000286824.6:c.648+23G>C	ENSP00000286824.6:n.648+23G>C
ENST00000378482.6:c.597+23G>C	ENSP00000367743.2:n.597+23G>C
ENST00000419600.3:n.541+23G>C
ENST00000465127.1:c.687+23G>C	ENSP00000417050.1:n.687+23G>C
ENST00000471410.5:c.*623+23G>C	ENSP00000419290.1:n.*623+23G>C
ENST00000475216.5:c.*590+23G>C	ENSP00000418586.1:n.*590+23G>C
NM_004615.3:c.597+23G>C	NP_004606.2:n.597+23G>C
NM_004615.4:c.597+23G>C MANE Select	NP_004606.2:n.597+23G>C