Canonical Allele Identifier: CA361664708

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148388537A>T (hg19) ; chr5:g.149008974A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008974A>T , CM000667.2:g.149008974A>T	GRCh38
NC_000005.9:g.148388537A>T , CM000667.1:g.148388537A>T	GRCh37
NC_000005.8:g.148368730A>T	NCBI36
NG_007947.2:g.59201T>A , LRG_269:g.59201T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3251T>A
ENST00000515425.6:c.3355T>A MANE Select	ENSP00000423660.1:p.Leu1119Met
ENST00000675793.1:c.*2639T>A	ENSP00000502039.1:n.*2639T>A
ENST00000323829.9:c.*2743T>A	ENSP00000313025.5:n.*2743T>A
ENST00000504517.5:c.2885T>A	ENSP00000421779.1:n.2885T>A
ENST00000504690.5:c.3355T>A	ENSP00000425627.1:p.Leu1119Met
ENST00000510779.1:c.2405T>A
ENST00000512049.5:c.3334T>A	ENSP00000421860.1:p.Leu1112Met
ENST00000515229.5:n.17T>A
ENST00000515425.5:c.3355T>A	ENSP00000423660.1:p.Leu1119Met
NM_024577.3:c.3355T>A , LRG_269t1:c.3355T>A	NP_078853.2:p.Leu1119Met
NM_024577.4:c.3355T>A MANE Select	NP_078853.2:p.Leu1119Met