Canonical Allele Identifier: CA2864103

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15567391C>T , CM000666.2:g.15567391C>T	GRCh38
NC_000004.11:g.15569014C>T , CM000666.1:g.15569014C>T	GRCh37
NC_000004.10:g.15178112C>T	NCBI36
NG_013035.1:g.102526C>T , LRG_697:g.102526C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378615.1:c.3197C>T MANE Select	NP_001365544.1:p.Pro1066Leu
ENST00000424120.6:c.3197C>T MANE Select	ENSP00000403465.1:p.Pro1066Leu
NM_001080522.2:c.3197C>T , LRG_697t1:c.3197C>T	NP_001073991.2:p.Pro1066Leu
NM_001378617.1:c.3050C>T	NP_001365546.1:p.Pro1017Leu
ENST00000389652.11:c.3212C>T	ENSP00000374303.8:p.Pro1071Leu
ENST00000389652.9:c.2674C>T
ENST00000424120.5:c.3197C>T	ENSP00000403465.1:p.Pro1066Leu
ENST00000503292.5:c.3197C>T	ENSP00000421809.1:p.Pro1066Leu
ENST00000503292.6:c.3197C>T	ENSP00000421809.1:p.Pro1066Leu
ENST00000506643.4:c.1525C>T
ENST00000506643.5:c.3050C>T	ENSP00000422931.2:p.Pro1017Leu
ENST00000634028.1:c.3180C>T	ENSP00000488669.1:n.3180C>T
ENST00000634028.2:c.3050C>T	ENSP00000488669.2:p.Pro1017Leu
ENST00000650860.2:c.*203C>T	ENSP00000498775.1:n.*203C>T
ENST00000674945.1:c.3050C>T	ENSP00000502333.1:p.Pro1017Leu
ENST00000675619.1:n.4008C>T
ENST00000675768.1:n.417C>T
ENST00000676337.1:c.*203C>T	ENSP00000501728.1:n.*203C>T
ENST00000680586.1:n.3856C>T
XM_005248177.1:c.3197C>T	XP_005248234.1:p.Pro1066Leu
XM_011513869.1:c.3197C>T	XP_011512171.1:p.Pro1066Leu
XM_011513870.1:c.3197C>T	XP_011512172.1:p.Pro1066Leu
XM_011513871.1:c.3050C>T	XP_011512173.1:p.Pro1017Leu
XM_017008482.1:c.3050C>T	XP_016863971.1:p.Pro1017Leu
XR_001741296.1:n.3442C>T