Canonical Allele Identifier: CA361664541

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148388461T>C (hg19) ; chr5:g.149008898T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008898T>C , CM000667.2:g.149008898T>C	GRCh38
NC_000005.9:g.148388461T>C , CM000667.1:g.148388461T>C	GRCh37
NC_000005.8:g.148368654T>C	NCBI36
NG_007947.2:g.59277A>G , LRG_269:g.59277A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3327A>G
ENST00000515425.6:c.3431A>G MANE Select	ENSP00000423660.1:p.Lys1144Arg
ENST00000675793.1:c.*2715A>G	ENSP00000502039.1:n.*2715A>G
ENST00000323829.9:c.*2819A>G	ENSP00000313025.5:n.*2819A>G
ENST00000504517.5:c.2961A>G	ENSP00000421779.1:n.2961A>G
ENST00000504690.5:c.3431A>G	ENSP00000425627.1:p.Lys1144Arg
ENST00000510779.1:c.2481A>G
ENST00000512049.5:c.3410A>G	ENSP00000421860.1:p.Lys1137Arg
ENST00000515229.5:n.93A>G
ENST00000515425.5:c.3431A>G	ENSP00000423660.1:p.Lys1144Arg
NM_024577.3:c.3431A>G , LRG_269t1:c.3431A>G	NP_078853.2:p.Lys1144Arg
NM_024577.4:c.3431A>G MANE Select	NP_078853.2:p.Lys1144Arg