Canonical Allele Identifier: CA447108030

Gene: SH3TC2

Linked Data

• gnomAD v4: 5-149026691-C-T
• MyVariant Identifiers: chr5:g.148406254C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026691C>T , CM000667.2:g.149026691C>T	GRCh38
NC_000005.9:g.148406254C>T , CM000667.1:g.148406254C>T	GRCh37
NC_000005.8:g.148386447C>T	NCBI36
NG_007947.2:g.41484G>A , LRG_269:g.41484G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2830G>A
ENST00000515425.6:c.2934G>A MANE Select	ENSP00000423660.1:p.Glu978=
ENST00000675793.1:c.*2218G>A	ENSP00000502039.1:n.*2218G>A
ENST00000676056.1:c.*2444G>A	ENSP00000501827.1:n.*2444G>A
ENST00000323829.9:c.*2322G>A	ENSP00000313025.5:n.*2322G>A
ENST00000504517.5:c.2464G>A	ENSP00000421779.1:n.2464G>A
ENST00000504690.5:c.2934G>A	ENSP00000425627.1:p.Glu978=
ENST00000510779.1:c.1984G>A
ENST00000511307.5:c.*2821G>A	ENSP00000421420.1:n.*2821G>A
ENST00000512049.5:c.2913G>A	ENSP00000421860.1:p.Glu971=
ENST00000513604.5:c.*2429G>A	ENSP00000423111.1:n.*2429G>A
ENST00000515425.5:c.2934G>A	ENSP00000423660.1:p.Glu978=
NM_024577.3:c.2934G>A , LRG_269t1:c.2934G>A	NP_078853.2:p.Glu978=
NM_024577.4:c.2934G>A MANE Select	NP_078853.2:p.Glu978=