Canonical Allele Identifier: CA361664238

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148386616G>T (hg19) ; chr5:g.149007053G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149007053G>T , CM000667.2:g.149007053G>T	GRCh38
NC_000005.9:g.148386616G>T , CM000667.1:g.148386616G>T	GRCh37
NC_000005.8:g.148366809G>T	NCBI36
NG_007947.2:g.61122C>A , LRG_269:g.61122C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.4356C>A
ENST00000515425.6:c.3503C>A MANE Select	ENSP00000423660.1:p.Ala1168Asp
ENST00000675793.1:c.*4560C>A	ENSP00000502039.1:n.*4560C>A
ENST00000323829.9:c.*2891C>A	ENSP00000313025.5:n.*2891C>A
ENST00000502274.1:c.89C>A	ENSP00000421092.1:p.Ala30Asp
ENST00000504517.5:c.3025C>A	ENSP00000421779.1:n.3025C>A
ENST00000504690.5:c.3503C>A	ENSP00000425627.1:p.Ala1168Asp
ENST00000510350.1:n.59C>A
ENST00000510779.1:c.2553C>A
ENST00000512049.5:c.3482C>A	ENSP00000421860.1:p.Ala1161Asp
ENST00000515229.5:n.165C>A
ENST00000515425.5:c.3503C>A	ENSP00000423660.1:p.Ala1168Asp
NM_024577.3:c.3503C>A , LRG_269t1:c.3503C>A	NP_078853.2:p.Ala1168Asp
NM_024577.4:c.3503C>A MANE Select	NP_078853.2:p.Ala1168Asp