Canonical Allele Identifier: CA361664652

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148388510T>G (hg19) ; chr5:g.149008947T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008947T>G , CM000667.2:g.149008947T>G	GRCh38
NC_000005.9:g.148388510T>G , CM000667.1:g.148388510T>G	GRCh37
NC_000005.8:g.148368703T>G	NCBI36
NG_007947.2:g.59228A>C , LRG_269:g.59228A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3278A>C
ENST00000515425.6:c.3382A>C MANE Select	ENSP00000423660.1:p.Ile1128Leu
ENST00000675793.1:c.*2666A>C	ENSP00000502039.1:n.*2666A>C
ENST00000323829.9:c.*2770A>C	ENSP00000313025.5:n.*2770A>C
ENST00000504517.5:c.2912A>C	ENSP00000421779.1:n.2912A>C
ENST00000504690.5:c.3382A>C	ENSP00000425627.1:p.Ile1128Leu
ENST00000510779.1:c.2432A>C
ENST00000512049.5:c.3361A>C	ENSP00000421860.1:p.Ile1121Leu
ENST00000515229.5:n.44A>C
ENST00000515425.5:c.3382A>C	ENSP00000423660.1:p.Ile1128Leu
NM_024577.3:c.3382A>C , LRG_269t1:c.3382A>C	NP_078853.2:p.Ile1128Leu
NM_024577.4:c.3382A>C MANE Select	NP_078853.2:p.Ile1128Leu