Canonical Allele Identifier: CA447395038

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148386615G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149007052G>C , CM000667.2:g.149007052G>C	GRCh38
NC_000005.9:g.148386615G>C , CM000667.1:g.148386615G>C	GRCh37
NC_000005.8:g.148366808G>C	NCBI36
NG_007947.2:g.61123C>G , LRG_269:g.61123C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.4357C>G
ENST00000515425.6:c.3504C>G MANE Select	ENSP00000423660.1:p.Ala1168=
ENST00000675793.1:c.*4561C>G	ENSP00000502039.1:n.*4561C>G
ENST00000323829.9:c.*2892C>G	ENSP00000313025.5:n.*2892C>G
ENST00000502274.1:c.90C>G	ENSP00000421092.1:p.Ala30=
ENST00000504517.5:c.3026C>G	ENSP00000421779.1:n.3026C>G
ENST00000504690.5:c.3504C>G	ENSP00000425627.1:p.Ala1168=
ENST00000510350.1:n.60C>G
ENST00000510779.1:c.2554C>G
ENST00000512049.5:c.3483C>G	ENSP00000421860.1:p.Ala1161=
ENST00000515229.5:n.166C>G
ENST00000515425.5:c.3504C>G	ENSP00000423660.1:p.Ala1168=
NM_024577.3:c.3504C>G , LRG_269t1:c.3504C>G	NP_078853.2:p.Ala1168=
NM_024577.4:c.3504C>G MANE Select	NP_078853.2:p.Ala1168=