Canonical Allele Identifier: CA361664567

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148388471C>G (hg19) ; chr5:g.149008908C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008908C>G , CM000667.2:g.149008908C>G	GRCh38
NC_000005.9:g.148388471C>G , CM000667.1:g.148388471C>G	GRCh37
NC_000005.8:g.148368664C>G	NCBI36
NG_007947.2:g.59267G>C , LRG_269:g.59267G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3317G>C
ENST00000515425.6:c.3421G>C MANE Select	ENSP00000423660.1:p.Gly1141Arg
ENST00000675793.1:c.*2705G>C	ENSP00000502039.1:n.*2705G>C
ENST00000323829.9:c.*2809G>C	ENSP00000313025.5:n.*2809G>C
ENST00000504517.5:c.2951G>C	ENSP00000421779.1:n.2951G>C
ENST00000504690.5:c.3421G>C	ENSP00000425627.1:p.Gly1141Arg
ENST00000510779.1:c.2471G>C
ENST00000512049.5:c.3400G>C	ENSP00000421860.1:p.Gly1134Arg
ENST00000515229.5:n.83G>C
ENST00000515425.5:c.3421G>C	ENSP00000423660.1:p.Gly1141Arg
NM_024577.3:c.3421G>C , LRG_269t1:c.3421G>C	NP_078853.2:p.Gly1141Arg
NM_024577.4:c.3421G>C MANE Select	NP_078853.2:p.Gly1141Arg