Canonical Allele Identifier: CA9015718

Gene: SHC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.438813C>T , CM000681.2:g.438813C>T	GRCh38
NC_000019.9:g.438813C>T , CM000681.1:g.438813C>T	GRCh37
NC_000019.8:g.389813C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264554.11:c.625G>A MANE Select	ENSP00000264554.4:p.Val209Ile
ENST00000264554.10:c.625G>A	ENSP00000264554.4:p.Val209Ile
ENST00000590113.4:n.121G>A
ENST00000590222.5:c.459G>A
NM_012435.2:c.625G>A	NP_036567.2:p.Val209Ile
XM_011527893.1:c.625G>A	XP_011526195.1:p.Val209Ile
XM_011527894.1:c.625G>A	XP_011526196.1:p.Val209Ile
XM_011527895.1:c.625G>A	XP_011526197.1:p.Val209Ile
XM_011527896.1:c.154G>A	XP_011526198.1:p.Val52Ile
XM_011527893.3:c.625G>A	XP_011526195.1:p.Val209Ile
XM_011527894.2:c.625G>A	XP_011526196.1:p.Val209Ile
XM_011527895.2:c.625G>A	XP_011526197.1:p.Val209Ile
XM_011527896.2:c.154G>A	XP_011526198.1:p.Val52Ile
NM_001387056.1:c.625G>A	NP_001373985.1:p.Val209Ile
NM_012435.3:c.625G>A MANE Select	NP_036567.2:p.Val209Ile