Canonical Allele Identifier: CA447107999

Gene: SH3TC2

Linked Data

• ClinVar Variation Id: 2006018
• ClinVar RCV Id: RCV002825647
• MyVariant Identifiers: chr5:g.148406197C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026634C>T , CM000667.2:g.149026634C>T	GRCh38
NC_000005.9:g.148406197C>T , CM000667.1:g.148406197C>T	GRCh37
NC_000005.8:g.148386390C>T	NCBI36
NG_007947.2:g.41541G>A , LRG_269:g.41541G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2887G>A
ENST00000515425.6:c.2991G>A MANE Select	ENSP00000423660.1:p.Arg997=
ENST00000675793.1:c.*2275G>A	ENSP00000502039.1:n.*2275G>A
ENST00000676056.1:c.*2501G>A	ENSP00000501827.1:n.*2501G>A
ENST00000323829.9:c.*2379G>A	ENSP00000313025.5:n.*2379G>A
ENST00000504517.5:c.2521G>A	ENSP00000421779.1:n.2521G>A
ENST00000504690.5:c.2991G>A	ENSP00000425627.1:p.Arg997=
ENST00000510779.1:c.2041G>A
ENST00000511307.5:c.*2878G>A	ENSP00000421420.1:n.*2878G>A
ENST00000512049.5:c.2970G>A	ENSP00000421860.1:p.Arg990=
ENST00000513604.5:c.*2486G>A	ENSP00000423111.1:n.*2486G>A
ENST00000515425.5:c.2991G>A	ENSP00000423660.1:p.Arg997=
NM_024577.3:c.2991G>A , LRG_269t1:c.2991G>A	NP_078853.2:p.Arg997=
NM_024577.4:c.2991G>A MANE Select	NP_078853.2:p.Arg997=