Canonical Allele Identifier: CA356429777

Gene: CC2D2A

Linked Data

• MyVariant Identifiers: chr4:g.15591240T>C (hg19) ; chr4:g.15589617T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15589617T>C , CM000666.2:g.15589617T>C	GRCh38
NC_000004.11:g.15591240T>C , CM000666.1:g.15591240T>C	GRCh37
NC_000004.10:g.15200338T>C	NCBI36
NG_013035.1:g.124752T>C , LRG_697:g.124752T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389652.11:c.4288T>C	ENSP00000374303.8:p.Tyr1430His
ENST00000424120.6:c.4252T>C MANE Select	ENSP00000403465.1:p.Tyr1418His
ENST00000503292.6:c.4252T>C	ENSP00000421809.1:p.Tyr1418His
ENST00000506643.5:c.4105T>C	ENSP00000422931.2:p.Tyr1369His
ENST00000514039.6:c.481T>C	ENSP00000488534.2:p.Tyr161His
ENST00000634028.2:c.4105T>C	ENSP00000488669.2:p.Tyr1369His
ENST00000650860.2:c.*1749T>C	ENSP00000498775.1:n.*1749T>C
ENST00000674945.1:c.3928T>C	ENSP00000502333.1:p.Tyr1310His
ENST00000675768.1:n.1472T>C
ENST00000680586.1:n.4911T>C
ENST00000389652.9:c.3750T>C
ENST00000424120.5:c.4252T>C	ENSP00000403465.1:p.Tyr1418His
ENST00000503292.5:c.4252T>C	ENSP00000421809.1:p.Tyr1418His
ENST00000506643.4:c.2580T>C
ENST00000634028.1:c.4058T>C	ENSP00000488669.1:n.4058T>C
NM_001080522.2:c.4252T>C , LRG_697t1:c.4252T>C	NP_001073991.2:p.Tyr1418His
XM_005248177.1:c.4252T>C	XP_005248234.1:p.Tyr1418His
XM_011513869.1:c.4270T>C	XP_011512171.1:p.Tyr1424His
XM_011513870.1:c.4270T>C	XP_011512172.1:p.Tyr1424His
XM_011513871.1:c.4123T>C	XP_011512173.1:p.Tyr1375His
XM_017008482.1:c.4105T>C	XP_016863971.1:p.Tyr1369His
NM_001378615.1:c.4252T>C MANE Select	NP_001365544.1:p.Tyr1418His
NM_001378617.1:c.4105T>C	NP_001365546.1:p.Tyr1369His