Canonical Allele Identifier: CA361667495

Gene: SH3TC2

Linked Data

• gnomAD v4: 5-149027832-T-C
• MyVariant Identifiers: chr5:g.148407395T>C (hg19) ; chr5:g.149027832T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027832T>C , CM000667.2:g.149027832T>C	GRCh38
NC_000005.9:g.148407395T>C , CM000667.1:g.148407395T>C	GRCh37
NC_000005.8:g.148387588T>C	NCBI36
NG_007947.2:g.40343A>G , LRG_269:g.40343A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1796A>G
ENST00000515425.6:c.1900A>G MANE Select	ENSP00000423660.1:p.Arg634Gly
ENST00000675793.1:c.*1184A>G	ENSP00000502039.1:n.*1184A>G
ENST00000676056.1:c.*1410A>G	ENSP00000501827.1:n.*1410A>G
ENST00000323829.9:c.*1288A>G	ENSP00000313025.5:n.*1288A>G
ENST00000504517.5:c.1430A>G	ENSP00000421779.1:n.1430A>G
ENST00000504690.5:c.1900A>G	ENSP00000425627.1:p.Arg634Gly
ENST00000510779.1:c.950A>G
ENST00000511307.5:c.*1680A>G	ENSP00000421420.1:n.*1680A>G
ENST00000512049.5:c.1879A>G	ENSP00000421860.1:p.Arg627Gly
ENST00000513604.5:c.*1288A>G	ENSP00000423111.1:n.*1288A>G
ENST00000515425.5:c.1900A>G	ENSP00000423660.1:p.Arg634Gly
NM_024577.3:c.1900A>G , LRG_269t1:c.1900A>G	NP_078853.2:p.Arg634Gly
NM_024577.4:c.1900A>G MANE Select	NP_078853.2:p.Arg634Gly