Canonical Allele Identifier: CA9015297

Gene: SHC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.422361G>C , CM000681.2:g.422361G>C	GRCh38
NC_000019.9:g.422361G>C , CM000681.1:g.422361G>C	GRCh37
NC_000019.8:g.373361G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264554.11:c.1405C>G MANE Select	ENSP00000264554.4:p.Pro469Ala
ENST00000264554.10:c.1405C>G	ENSP00000264554.4:p.Pro469Ala
ENST00000588376.5:n.468C>G
ENST00000590170.3:c.344C>G
NM_012435.2:c.1405C>G	NP_036567.2:p.Pro469Ala
XM_011527893.1:c.1405C>G	XP_011526195.1:p.Pro469Ala
XM_011527894.1:c.1270C>G	XP_011526196.1:p.Pro424Ala
XM_011527895.1:c.1270C>G	XP_011526197.1:p.Pro424Ala
XM_011527896.1:c.934C>G	XP_011526198.1:p.Pro312Ala
XM_011527893.3:c.1405C>G	XP_011526195.1:p.Pro469Ala
XM_011527894.2:c.1270C>G	XP_011526196.1:p.Pro424Ala
XM_011527895.2:c.1270C>G	XP_011526197.1:p.Pro424Ala
XM_011527896.2:c.934C>G	XP_011526198.1:p.Pro312Ala
NM_001387056.1:c.1270C>G	NP_001373985.1:p.Pro424Ala
NM_012435.3:c.1405C>G MANE Select	NP_036567.2:p.Pro469Ala