Canonical Allele Identifier: CA361665122

Gene: SH3TC2

Linked Data

• gnomAD v4: 5-149026610-C-A
• MyVariant Identifiers: chr5:g.148406173C>A (hg19) ; chr5:g.149026610C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026610C>A , CM000667.2:g.149026610C>A	GRCh38
NC_000005.9:g.148406173C>A , CM000667.1:g.148406173C>A	GRCh37
NC_000005.8:g.148386366C>A	NCBI36
NG_007947.2:g.41565G>T , LRG_269:g.41565G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2911G>T
ENST00000515425.6:c.3015G>T MANE Select	ENSP00000423660.1:p.Glu1005Asp
ENST00000675793.1:c.*2299G>T	ENSP00000502039.1:n.*2299G>T
ENST00000676056.1:c.*2525G>T	ENSP00000501827.1:n.*2525G>T
ENST00000323829.9:c.*2403G>T	ENSP00000313025.5:n.*2403G>T
ENST00000504517.5:c.2545G>T	ENSP00000421779.1:n.2545G>T
ENST00000504690.5:c.3015G>T	ENSP00000425627.1:p.Glu1005Asp
ENST00000510779.1:c.2065G>T
ENST00000511307.5:c.*2902G>T	ENSP00000421420.1:n.*2902G>T
ENST00000512049.5:c.2994G>T	ENSP00000421860.1:p.Glu998Asp
ENST00000513604.5:c.*2510G>T	ENSP00000423111.1:n.*2510G>T
ENST00000515425.5:c.3015G>T	ENSP00000423660.1:p.Glu1005Asp
NM_024577.3:c.3015G>T , LRG_269t1:c.3015G>T	NP_078853.2:p.Glu1005Asp
NM_024577.4:c.3015G>T MANE Select	NP_078853.2:p.Glu1005Asp