Canonical Allele Identifier: CA402893571

Gene: SHC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.440880G>C , CM000681.2:g.440880G>C	GRCh38
NC_000019.9:g.440880G>C , CM000681.1:g.440880G>C	GRCh37
NC_000019.8:g.391880G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264554.11:c.521C>G MANE Select	ENSP00000264554.4:p.Thr174Arg
ENST00000264554.10:c.521C>G	ENSP00000264554.4:p.Thr174Arg
ENST00000590222.5:c.96C>G
NM_012435.2:c.521C>G	NP_036567.2:p.Thr174Arg
XM_011527893.1:c.521C>G	XP_011526195.1:p.Thr174Arg
XM_011527894.1:c.521C>G	XP_011526196.1:p.Thr174Arg
XM_011527895.1:c.521C>G	XP_011526197.1:p.Thr174Arg
XM_011527896.1:c.50C>G	XP_011526198.1:p.Thr17Arg
XM_011527893.3:c.521C>G	XP_011526195.1:p.Thr174Arg
XM_011527894.2:c.521C>G	XP_011526196.1:p.Thr174Arg
XM_011527895.2:c.521C>G	XP_011526197.1:p.Thr174Arg
XM_011527896.2:c.50C>G	XP_011526198.1:p.Thr17Arg
NM_001387056.1:c.521C>G	NP_001373985.1:p.Thr174Arg
NM_012435.3:c.521C>G MANE Select	NP_036567.2:p.Thr174Arg