Canonical Allele Identifier: CA356433912

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15599587T>C , CM000666.2:g.15599587T>C	GRCh38
NC_000004.11:g.15601210T>C , CM000666.1:g.15601210T>C	GRCh37
NC_000004.10:g.15210308T>C	NCBI36
NG_013035.1:g.134722T>C , LRG_697:g.134722T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001378615.1:c.4555T>C MANE Select	NP_001365544.1:p.Trp1519Arg
ENST00000424120.6:c.4555T>C MANE Select	ENSP00000403465.1:p.Trp1519Arg
NM_001080522.2:c.4555T>C , LRG_697t1:c.4555T>C	NP_001073991.2:p.Trp1519Arg
NM_001378617.1:c.4408T>C	NP_001365546.1:p.Trp1470Arg
ENST00000389652.11:c.4591T>C	ENSP00000374303.8:p.Trp1531Arg
ENST00000389652.9:c.4053T>C
ENST00000424120.5:c.4555T>C	ENSP00000403465.1:p.Trp1519Arg
ENST00000503292.5:c.4555T>C	ENSP00000421809.1:p.Trp1519Arg
ENST00000503292.6:c.4555T>C	ENSP00000421809.1:p.Trp1519Arg
ENST00000506643.4:c.2824T>C
ENST00000506643.5:c.4408T>C	ENSP00000422931.2:p.Trp1470Arg
ENST00000514039.5:c.171T>C
ENST00000514039.6:c.661T>C	ENSP00000488534.2:p.Trp221Arg
ENST00000634028.1:c.4361T>C	ENSP00000488669.1:n.4361T>C
ENST00000634028.2:c.4349T>C	ENSP00000488669.2:n.4349T>C
ENST00000650860.2:c.*2052T>C	ENSP00000498775.1:n.*2052T>C
ENST00000674945.1:c.4231T>C	ENSP00000502333.1:p.Trp1411Arg
ENST00000680586.1:n.5214T>C
XM_005248177.1:c.4555T>C	XP_005248234.1:p.Trp1519Arg
XM_011513869.1:c.4573T>C	XP_011512171.1:p.Trp1525Arg
XM_011513870.1:c.4573T>C	XP_011512172.1:p.Trp1525Arg
XM_011513871.1:c.4426T>C	XP_011512173.1:p.Trp1476Arg
XM_017008482.1:c.4408T>C	XP_016863971.1:p.Trp1470Arg