Canonical Allele Identifier: CA447108032

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148406257A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026694A>G , CM000667.2:g.149026694A>G	GRCh38
NC_000005.9:g.148406257A>G , CM000667.1:g.148406257A>G	GRCh37
NC_000005.8:g.148386450A>G	NCBI36
NG_007947.2:g.41481T>C , LRG_269:g.41481T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2827T>C
ENST00000515425.6:c.2931T>C MANE Select	ENSP00000423660.1:p.Pro977=
ENST00000675793.1:c.*2215T>C	ENSP00000502039.1:n.*2215T>C
ENST00000676056.1:c.*2441T>C	ENSP00000501827.1:n.*2441T>C
ENST00000323829.9:c.*2319T>C	ENSP00000313025.5:n.*2319T>C
ENST00000504517.5:c.2461T>C	ENSP00000421779.1:n.2461T>C
ENST00000504690.5:c.2931T>C	ENSP00000425627.1:p.Pro977=
ENST00000510779.1:c.1981T>C
ENST00000511307.5:c.*2818T>C	ENSP00000421420.1:n.*2818T>C
ENST00000512049.5:c.2910T>C	ENSP00000421860.1:p.Pro970=
ENST00000513604.5:c.*2426T>C	ENSP00000423111.1:n.*2426T>C
ENST00000515425.5:c.2931T>C	ENSP00000423660.1:p.Pro977=
NM_024577.3:c.2931T>C , LRG_269t1:c.2931T>C	NP_078853.2:p.Pro977=
NM_024577.4:c.2931T>C MANE Select	NP_078853.2:p.Pro977=