Canonical Allele Identifier: CA356418592

Gene: CC2D2A

Linked Data

• MyVariant Identifiers: chr4:g.15569307T>G (hg19) ; chr4:g.15567684T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15567684T>G , CM000666.2:g.15567684T>G	GRCh38
NC_000004.11:g.15569307T>G , CM000666.1:g.15569307T>G	GRCh37
NC_000004.10:g.15178405T>G	NCBI36
NG_013035.1:g.102819T>G , LRG_697:g.102819T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389652.11:c.3311T>G	ENSP00000374303.8:p.Val1104Gly
ENST00000424120.6:c.3296T>G MANE Select	ENSP00000403465.1:p.Val1099Gly
ENST00000503292.6:c.3296T>G	ENSP00000421809.1:p.Val1099Gly
ENST00000506643.5:c.3149T>G	ENSP00000422931.2:p.Val1050Gly
ENST00000634028.2:c.3149T>G	ENSP00000488669.2:p.Val1050Gly
ENST00000650860.2:c.*302T>G	ENSP00000498775.1:n.*302T>G
ENST00000674945.1:c.3149T>G	ENSP00000502333.1:p.Val1050Gly
ENST00000675619.1:n.4107T>G
ENST00000675768.1:n.516T>G
ENST00000676337.1:c.*302T>G	ENSP00000501728.1:n.*302T>G
ENST00000680586.1:n.3955T>G
ENST00000389652.9:c.2773T>G
ENST00000424120.5:c.3296T>G	ENSP00000403465.1:p.Val1099Gly
ENST00000503292.5:c.3296T>G	ENSP00000421809.1:p.Val1099Gly
ENST00000506643.4:c.1624T>G
ENST00000634028.1:c.3279T>G	ENSP00000488669.1:n.3279T>G
NM_001080522.2:c.3296T>G , LRG_697t1:c.3296T>G	NP_001073991.2:p.Val1099Gly
XM_005248177.1:c.3296T>G	XP_005248234.1:p.Val1099Gly
XM_011513869.1:c.3296T>G	XP_011512171.1:p.Val1099Gly
XM_011513870.1:c.3296T>G	XP_011512172.1:p.Val1099Gly
XM_011513871.1:c.3149T>G	XP_011512173.1:p.Val1050Gly
XM_017008482.1:c.3149T>G	XP_016863971.1:p.Val1050Gly
XR_001741296.1:n.3541T>G
NM_001378615.1:c.3296T>G MANE Select	NP_001365544.1:p.Val1099Gly
NM_001378617.1:c.3149T>G	NP_001365546.1:p.Val1050Gly