Canonical Allele Identifier: CA361664487

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148388434G>T (hg19) ; chr5:g.149008871G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008871G>T , CM000667.2:g.149008871G>T	GRCh38
NC_000005.9:g.148388434G>T , CM000667.1:g.148388434G>T	GRCh37
NC_000005.8:g.148368627G>T	NCBI36
NG_007947.2:g.59304C>A , LRG_269:g.59304C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3354C>A
ENST00000515425.6:c.3458C>A MANE Select	ENSP00000423660.1:p.Ala1153Asp
ENST00000675793.1:c.*2742C>A	ENSP00000502039.1:n.*2742C>A
ENST00000323829.9:c.*2846C>A	ENSP00000313025.5:n.*2846C>A
ENST00000504517.5:c.2988C>A	ENSP00000421779.1:n.2988C>A
ENST00000504690.5:c.3458C>A	ENSP00000425627.1:p.Ala1153Asp
ENST00000510779.1:c.2508C>A
ENST00000512049.5:c.3437C>A	ENSP00000421860.1:p.Ala1146Asp
ENST00000515229.5:n.120C>A
ENST00000515425.5:c.3458C>A	ENSP00000423660.1:p.Ala1153Asp
NM_024577.3:c.3458C>A , LRG_269t1:c.3458C>A	NP_078853.2:p.Ala1153Asp
NM_024577.4:c.3458C>A MANE Select	NP_078853.2:p.Ala1153Asp