Canonical Allele Identifier: CA361665112

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148406168A>T (hg19) ; chr5:g.149026605A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026605A>T , CM000667.2:g.149026605A>T	GRCh38
NC_000005.9:g.148406168A>T , CM000667.1:g.148406168A>T	GRCh37
NC_000005.8:g.148386361A>T	NCBI36
NG_007947.2:g.41570T>A , LRG_269:g.41570T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2916T>A
ENST00000515425.6:c.3020T>A MANE Select	ENSP00000423660.1:p.Leu1007Gln
ENST00000675793.1:c.*2304T>A	ENSP00000502039.1:n.*2304T>A
ENST00000676056.1:c.*2530T>A	ENSP00000501827.1:n.*2530T>A
ENST00000323829.9:c.*2408T>A	ENSP00000313025.5:n.*2408T>A
ENST00000504517.5:c.2550T>A	ENSP00000421779.1:n.2550T>A
ENST00000504690.5:c.3020T>A	ENSP00000425627.1:p.Leu1007Gln
ENST00000510779.1:c.2070T>A
ENST00000511307.5:c.*2907T>A	ENSP00000421420.1:n.*2907T>A
ENST00000512049.5:c.2999T>A	ENSP00000421860.1:p.Leu1000Gln
ENST00000513604.5:c.*2515T>A	ENSP00000423111.1:n.*2515T>A
ENST00000515425.5:c.3020T>A	ENSP00000423660.1:p.Leu1007Gln
NM_024577.3:c.3020T>A , LRG_269t1:c.3020T>A	NP_078853.2:p.Leu1007Gln
NM_024577.4:c.3020T>A MANE Select	NP_078853.2:p.Leu1007Gln