Canonical Allele Identifier: CA9015814

Gene: SHC2

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264554.11:c.521C>T MANE Select	ENSP00000264554.4:p.Thr174Met
ENST00000264554.10:c.521C>T	ENSP00000264554.4:p.Thr174Met
ENST00000590222.5:c.96C>T
NM_012435.2:c.521C>T	NP_036567.2:p.Thr174Met
XM_011527893.1:c.521C>T	XP_011526195.1:p.Thr174Met
XM_011527894.1:c.521C>T	XP_011526196.1:p.Thr174Met
XM_011527895.1:c.521C>T	XP_011526197.1:p.Thr174Met
XM_011527896.1:c.50C>T	XP_011526198.1:p.Thr17Met
XM_011527893.3:c.521C>T	XP_011526195.1:p.Thr174Met
XM_011527894.2:c.521C>T	XP_011526196.1:p.Thr174Met
XM_011527895.2:c.521C>T	XP_011526197.1:p.Thr174Met
XM_011527896.2:c.50C>T	XP_011526198.1:p.Thr17Met
NM_001387056.1:c.521C>T	NP_001373985.1:p.Thr174Met
NM_012435.3:c.521C>T MANE Select	NP_036567.2:p.Thr174Met