Canonical Allele Identifier: CA438382318

Gene: CC2D2A

Linked Data

• MyVariant Identifiers: chr4:g.15560803T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15559180T>C , CM000666.2:g.15559180T>C	GRCh38
NC_000004.11:g.15560803T>C , CM000666.1:g.15560803T>C	GRCh37
NC_000004.10:g.15169901T>C	NCBI36
NG_013035.1:g.94315T>C , LRG_697:g.94315T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389652.11:c.2845T>C	ENSP00000374303.8:p.Leu949=
ENST00000424120.6:c.2845T>C MANE Select	ENSP00000403465.1:p.Leu949=
ENST00000503292.6:c.2845T>C	ENSP00000421809.1:p.Leu949=
ENST00000506643.5:c.2698T>C	ENSP00000422931.2:p.Leu900=
ENST00000634028.2:c.2698T>C	ENSP00000488669.2:p.Leu900=
ENST00000650860.2:c.2698T>C	ENSP00000498775.1:p.Leu900=
ENST00000674945.1:c.2698T>C	ENSP00000502333.1:p.Leu900=
ENST00000675619.1:n.924T>C
ENST00000675768.1:n.65T>C
ENST00000676337.1:c.2698T>C	ENSP00000501728.1:p.Leu900=
ENST00000680586.1:n.772T>C
ENST00000389652.9:c.2307T>C
ENST00000424120.5:c.2845T>C	ENSP00000403465.1:p.Leu949=
ENST00000503292.5:c.2845T>C	ENSP00000421809.1:p.Leu949=
ENST00000506643.4:c.1173T>C
ENST00000634028.1:c.2828T>C	ENSP00000488669.1:n.2828T>C
NM_001080522.2:c.2845T>C , LRG_697t1:c.2845T>C	NP_001073991.2:p.Leu949=
XM_005248177.1:c.2845T>C	XP_005248234.1:p.Leu949=
XM_011513869.1:c.2845T>C	XP_011512171.1:p.Leu949=
XM_011513870.1:c.2845T>C	XP_011512172.1:p.Leu949=
XM_011513871.1:c.2698T>C	XP_011512173.1:p.Leu900=
XM_011513872.1:c.2845T>C	XP_011512174.1:p.Leu949=
XM_011513873.1:c.2845T>C	XP_011512175.1:p.Leu949=
XM_011513872.3:c.2845T>C	XP_011512174.1:p.Leu949=
XM_017008482.1:c.2698T>C	XP_016863971.1:p.Leu900=
XR_001741296.1:n.3045T>C
NM_001378615.1:c.2845T>C MANE Select	NP_001365544.1:p.Leu949=
NM_001378617.1:c.2698T>C	NP_001365546.1:p.Leu900=