Canonical Allele Identifier: CA361665047

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148406136T>A (hg19) ; chr5:g.149026573T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026573T>A , CM000667.2:g.149026573T>A	GRCh38
NC_000005.9:g.148406136T>A , CM000667.1:g.148406136T>A	GRCh37
NC_000005.8:g.148386329T>A	NCBI36
NG_007947.2:g.41602A>T , LRG_269:g.41602A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2948A>T
ENST00000515425.6:c.3052A>T MANE Select	ENSP00000423660.1:p.Arg1018Trp
ENST00000675793.1:c.*2336A>T	ENSP00000502039.1:n.*2336A>T
ENST00000676056.1:c.*2562A>T	ENSP00000501827.1:n.*2562A>T
ENST00000323829.9:c.*2440A>T	ENSP00000313025.5:n.*2440A>T
ENST00000504517.5:c.2582A>T	ENSP00000421779.1:n.2582A>T
ENST00000504690.5:c.3052A>T	ENSP00000425627.1:p.Arg1018Trp
ENST00000510779.1:c.2102A>T
ENST00000511307.5:c.*2939A>T	ENSP00000421420.1:n.*2939A>T
ENST00000512049.5:c.3031A>T	ENSP00000421860.1:p.Arg1011Trp
ENST00000513604.5:c.*2547A>T	ENSP00000423111.1:n.*2547A>T
ENST00000515425.5:c.3052A>T	ENSP00000423660.1:p.Arg1018Trp
NM_024577.3:c.3052A>T , LRG_269t1:c.3052A>T	NP_078853.2:p.Arg1018Trp
NM_024577.4:c.3052A>T MANE Select	NP_078853.2:p.Arg1018Trp