Canonical Allele Identifier: CA2675887400

Gene: SH3TC2

Linked Data

• gnomAD v4: 5-149008659-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008659C>A , CM000667.2:g.149008659C>A	GRCh38
NC_000005.9:g.148388222C>A , CM000667.1:g.148388222C>A	GRCh37
NC_000005.8:g.148368415C>A	NCBI36
NG_007947.2:g.59516G>T , LRG_269:g.59516G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3374+192G>T
ENST00000515425.6:c.3478+192G>T MANE Select	ENSP00000423660.1:n.3478+192G>T
ENST00000675793.1:c.*2954G>T	ENSP00000502039.1:n.*2954G>T
ENST00000323829.9:c.*2866+192G>T	ENSP00000313025.5:n.*2866+192G>T
ENST00000504517.5:c.3008+192G>T	ENSP00000421779.1:n.3008+192G>T
ENST00000504690.5:c.3478+192G>T	ENSP00000425627.1:n.3478+192G>T
ENST00000510779.1:c.2528+192G>T
ENST00000512049.5:c.3457+192G>T	ENSP00000421860.1:n.3457+192G>T
ENST00000515229.5:n.140+192G>T
ENST00000515425.5:c.3478+192G>T	ENSP00000423660.1:n.3478+192G>T
NM_024577.3:c.3478+192G>T , LRG_269t1:c.3478+192G>T	NP_078853.2:n.3478+192G>T
NM_024577.4:c.3478+192G>T MANE Select	NP_078853.2:n.3478+192G>T