Canonical Allele Identifier: CA361664231

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148386612A>T (hg19) ; chr5:g.149007049A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149007049A>T , CM000667.2:g.149007049A>T	GRCh38
NC_000005.9:g.148386612A>T , CM000667.1:g.148386612A>T	GRCh37
NC_000005.8:g.148366805A>T	NCBI36
NG_007947.2:g.61126T>A , LRG_269:g.61126T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.4360T>A
ENST00000515425.6:c.3507T>A MANE Select	ENSP00000423660.1:p.Phe1169Leu
ENST00000675793.1:c.*4564T>A	ENSP00000502039.1:n.*4564T>A
ENST00000323829.9:c.*2895T>A	ENSP00000313025.5:n.*2895T>A
ENST00000502274.1:c.93T>A	ENSP00000421092.1:p.Phe31Leu
ENST00000504517.5:c.3029T>A	ENSP00000421779.1:n.3029T>A
ENST00000504690.5:c.3507T>A	ENSP00000425627.1:p.Phe1169Leu
ENST00000510350.1:n.63T>A
ENST00000510779.1:c.2557T>A
ENST00000512049.5:c.3486T>A	ENSP00000421860.1:p.Phe1162Leu
ENST00000515229.5:n.169T>A
ENST00000515425.5:c.3507T>A	ENSP00000423660.1:p.Phe1169Leu
NM_024577.3:c.3507T>A , LRG_269t1:c.3507T>A	NP_078853.2:p.Phe1169Leu
NM_024577.4:c.3507T>A MANE Select	NP_078853.2:p.Phe1169Leu