Canonical Allele Identifier: CA361667702

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407496G>A (hg19) ; chr5:g.149027933G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027933G>A , CM000667.2:g.149027933G>A	GRCh38
NC_000005.9:g.148407496G>A , CM000667.1:g.148407496G>A	GRCh37
NC_000005.8:g.148387689G>A	NCBI36
NG_007947.2:g.40242C>T , LRG_269:g.40242C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.1695C>T
ENST00000515425.6:c.1799C>T MANE Select	ENSP00000423660.1:p.Ala600Val
ENST00000675793.1:c.*1083C>T	ENSP00000502039.1:n.*1083C>T
ENST00000676056.1:c.*1309C>T	ENSP00000501827.1:n.*1309C>T
ENST00000323829.9:c.*1187C>T	ENSP00000313025.5:n.*1187C>T
ENST00000504517.5:c.1329C>T	ENSP00000421779.1:n.1329C>T
ENST00000504690.5:c.1799C>T	ENSP00000425627.1:p.Ala600Val
ENST00000510779.1:c.849C>T
ENST00000511307.5:c.*1579C>T	ENSP00000421420.1:n.*1579C>T
ENST00000512049.5:c.1778C>T	ENSP00000421860.1:p.Ala593Val
ENST00000513604.5:c.*1187C>T	ENSP00000423111.1:n.*1187C>T
ENST00000515425.5:c.1799C>T	ENSP00000423660.1:p.Ala600Val
NM_024577.3:c.1799C>T , LRG_269t1:c.1799C>T	NP_078853.2:p.Ala600Val
NM_024577.4:c.1799C>T MANE Select	NP_078853.2:p.Ala600Val