Canonical Allele Identifier: CA361667984

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407611A>C (hg19) ; chr5:g.149028048A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149028048A>C , CM000667.2:g.149028048A>C	GRCh38
NC_000005.9:g.148407611A>C , CM000667.1:g.148407611A>C	GRCh37
NC_000005.8:g.148387804A>C	NCBI36
NG_007947.2:g.40127T>G , LRG_269:g.40127T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.1580T>G
ENST00000515425.6:c.1684T>G MANE Select	ENSP00000423660.1:p.Phe562Val
ENST00000675793.1:c.*968T>G	ENSP00000502039.1:n.*968T>G
ENST00000676056.1:c.*1194T>G	ENSP00000501827.1:n.*1194T>G
ENST00000323829.9:c.*1072T>G	ENSP00000313025.5:n.*1072T>G
ENST00000504517.5:c.1214T>G	ENSP00000421779.1:n.1214T>G
ENST00000504690.5:c.1684T>G	ENSP00000425627.1:p.Phe562Val
ENST00000510779.1:c.734T>G
ENST00000511307.5:c.*1464T>G	ENSP00000421420.1:n.*1464T>G
ENST00000512049.5:c.1663T>G	ENSP00000421860.1:p.Phe555Val
ENST00000513604.5:c.*1072T>G	ENSP00000423111.1:n.*1072T>G
ENST00000515425.5:c.1684T>G	ENSP00000423660.1:p.Phe562Val
NM_024577.3:c.1684T>G , LRG_269t1:c.1684T>G	NP_078853.2:p.Phe562Val
NM_024577.4:c.1684T>G MANE Select	NP_078853.2:p.Phe562Val