Canonical Allele Identifier: CA361665374

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148406288C>G (hg19) ; chr5:g.149026725C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026725C>G , CM000667.2:g.149026725C>G	GRCh38
NC_000005.9:g.148406288C>G , CM000667.1:g.148406288C>G	GRCh37
NC_000005.8:g.148386481C>G	NCBI36
NG_007947.2:g.41450G>C , LRG_269:g.41450G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2796G>C
ENST00000515425.6:c.2900G>C MANE Select	ENSP00000423660.1:p.Cys967Ser
ENST00000675793.1:c.*2184G>C	ENSP00000502039.1:n.*2184G>C
ENST00000676056.1:c.*2410G>C	ENSP00000501827.1:n.*2410G>C
ENST00000323829.9:c.*2288G>C	ENSP00000313025.5:n.*2288G>C
ENST00000504517.5:c.2430G>C	ENSP00000421779.1:n.2430G>C
ENST00000504690.5:c.2900G>C	ENSP00000425627.1:p.Cys967Ser
ENST00000510779.1:c.1950G>C
ENST00000511307.5:c.*2787G>C	ENSP00000421420.1:n.*2787G>C
ENST00000512049.5:c.2879G>C	ENSP00000421860.1:p.Cys960Ser
ENST00000513604.5:c.*2395G>C	ENSP00000423111.1:n.*2395G>C
ENST00000515425.5:c.2900G>C	ENSP00000423660.1:p.Cys967Ser
NM_024577.3:c.2900G>C , LRG_269t1:c.2900G>C	NP_078853.2:p.Cys967Ser
NM_024577.4:c.2900G>C MANE Select	NP_078853.2:p.Cys967Ser