Canonical Allele Identifier: CA361665146

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148406187C>A (hg19) ; chr5:g.149026624C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026624C>A , CM000667.2:g.149026624C>A	GRCh38
NC_000005.9:g.148406187C>A , CM000667.1:g.148406187C>A	GRCh37
NC_000005.8:g.148386380C>A	NCBI36
NG_007947.2:g.41551G>T , LRG_269:g.41551G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2897G>T
ENST00000515425.6:c.3001G>T MANE Select	ENSP00000423660.1:p.Gly1001Trp
ENST00000675793.1:c.*2285G>T	ENSP00000502039.1:n.*2285G>T
ENST00000676056.1:c.*2511G>T	ENSP00000501827.1:n.*2511G>T
ENST00000323829.9:c.*2389G>T	ENSP00000313025.5:n.*2389G>T
ENST00000504517.5:c.2531G>T	ENSP00000421779.1:n.2531G>T
ENST00000504690.5:c.3001G>T	ENSP00000425627.1:p.Gly1001Trp
ENST00000510779.1:c.2051G>T
ENST00000511307.5:c.*2888G>T	ENSP00000421420.1:n.*2888G>T
ENST00000512049.5:c.2980G>T	ENSP00000421860.1:p.Gly994Trp
ENST00000513604.5:c.*2496G>T	ENSP00000423111.1:n.*2496G>T
ENST00000515425.5:c.3001G>T	ENSP00000423660.1:p.Gly1001Trp
NM_024577.3:c.3001G>T , LRG_269t1:c.3001G>T	NP_078853.2:p.Gly1001Trp
NM_024577.4:c.3001G>T MANE Select	NP_078853.2:p.Gly1001Trp