Canonical Allele Identifier: CA361667136

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407221A>C (hg19) ; chr5:g.149027658A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027658A>C , CM000667.2:g.149027658A>C	GRCh38
NC_000005.9:g.148407221A>C , CM000667.1:g.148407221A>C	GRCh37
NC_000005.8:g.148387414A>C	NCBI36
NG_007947.2:g.40517T>G , LRG_269:g.40517T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1970T>G
ENST00000515425.6:c.2074T>G MANE Select	ENSP00000423660.1:p.Ser692Ala
ENST00000675793.1:c.*1358T>G	ENSP00000502039.1:n.*1358T>G
ENST00000676056.1:c.*1584T>G	ENSP00000501827.1:n.*1584T>G
ENST00000323829.9:c.*1462T>G	ENSP00000313025.5:n.*1462T>G
ENST00000504517.5:c.1604T>G	ENSP00000421779.1:n.1604T>G
ENST00000504690.5:c.2074T>G	ENSP00000425627.1:p.Ser692Ala
ENST00000510779.1:c.1124T>G
ENST00000511307.5:c.*1854T>G	ENSP00000421420.1:n.*1854T>G
ENST00000512049.5:c.2053T>G	ENSP00000421860.1:p.Ser685Ala
ENST00000513604.5:c.*1462T>G	ENSP00000423111.1:n.*1462T>G
ENST00000515425.5:c.2074T>G	ENSP00000423660.1:p.Ser692Ala
NM_024577.3:c.2074T>G , LRG_269t1:c.2074T>G	NP_078853.2:p.Ser692Ala
NM_024577.4:c.2074T>G MANE Select	NP_078853.2:p.Ser692Ala