Canonical Allele Identifier: CA361664751

Gene: SH3TC2

Linked Data

• gnomAD v4: 5-149008995-C-T
• MyVariant Identifiers: chr5:g.148388558C>T (hg19) ; chr5:g.149008995C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008995C>T , CM000667.2:g.149008995C>T	GRCh38
NC_000005.9:g.148388558C>T , CM000667.1:g.148388558C>T	GRCh37
NC_000005.8:g.148368751C>T	NCBI36
NG_007947.2:g.59180G>A , LRG_269:g.59180G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3230G>A
ENST00000515425.6:c.3334G>A MANE Select	ENSP00000423660.1:p.Ala1112Thr
ENST00000675793.1:c.*2618G>A	ENSP00000502039.1:n.*2618G>A
ENST00000323829.9:c.*2722G>A	ENSP00000313025.5:n.*2722G>A
ENST00000504517.5:c.2864G>A	ENSP00000421779.1:n.2864G>A
ENST00000504690.5:c.3334G>A	ENSP00000425627.1:p.Ala1112Thr
ENST00000510779.1:c.2384G>A
ENST00000512049.5:c.3313G>A	ENSP00000421860.1:p.Ala1105Thr
ENST00000515425.5:c.3334G>A	ENSP00000423660.1:p.Ala1112Thr
NM_024577.3:c.3334G>A , LRG_269t1:c.3334G>A	NP_078853.2:p.Ala1112Thr
NM_024577.4:c.3334G>A MANE Select	NP_078853.2:p.Ala1112Thr