Canonical Allele Identifier: CA2675887543

Gene: SH3TC2

Linked Data

• gnomAD v4: 5-149009027-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149009027T>C , CM000667.2:g.149009027T>C	GRCh38
NC_000005.9:g.148388590T>C , CM000667.1:g.148388590T>C	GRCh37
NC_000005.8:g.148368783T>C	NCBI36
NG_007947.2:g.59148A>G , LRG_269:g.59148A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3224-26A>G
ENST00000515425.6:c.3328-26A>G MANE Select	ENSP00000423660.1:n.3328-26A>G
ENST00000675793.1:c.*2612-26A>G	ENSP00000502039.1:n.*2612-26A>G
ENST00000323829.9:c.*2716-26A>G	ENSP00000313025.5:n.*2716-26A>G
ENST00000504517.5:c.2858-26A>G	ENSP00000421779.1:n.2858-26A>G
ENST00000504690.5:c.3328-26A>G	ENSP00000425627.1:n.3328-26A>G
ENST00000510779.1:c.2378-26A>G
ENST00000512049.5:c.3307-26A>G	ENSP00000421860.1:n.3307-26A>G
ENST00000515425.5:c.3328-26A>G	ENSP00000423660.1:n.3328-26A>G
NM_024577.3:c.3328-26A>G , LRG_269t1:c.3328-26A>G	NP_078853.2:n.3328-26A>G
NM_024577.4:c.3328-26A>G MANE Select	NP_078853.2:n.3328-26A>G