Canonical Allele Identifier: CA2864250

Gene: CC2D2A

Linked Data

• ClinVar Variation Id: 421683
• ClinVar RCV Id: RCV000726978 ; RCV000765762 ; RCV001081324 ; RCV003932778
• dbSNP Id: rs200427832
• ExAC: 4:15581688 T / C
• gnomAD v2: 4-15581688-T-C
• gnomAD v3: 4-15580065-T-C
• gnomAD v4: 4-15580065-T-C
• MyVariant Identifiers: chr4:g.15581688T>C (hg19) ; chr4:g.15580065T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15580065T>C , CM000666.2:g.15580065T>C	GRCh38
NC_000004.11:g.15581688T>C , CM000666.1:g.15581688T>C	GRCh37
NC_000004.10:g.15190786T>C	NCBI36
NG_013035.1:g.115200T>C , LRG_697:g.115200T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000389652.11:c.3905T>C	ENSP00000374303.8:p.Val1302Ala
ENST00000424120.6:c.3869T>C MANE Select	ENSP00000403465.1:p.Val1290Ala
ENST00000503292.6:c.3869T>C	ENSP00000421809.1:p.Val1290Ala
ENST00000506643.5:c.3722T>C	ENSP00000422931.2:p.Val1241Ala
ENST00000514039.6:c.98T>C	ENSP00000488534.2:p.Val33Ala
ENST00000634028.2:c.3722T>C	ENSP00000488669.2:p.Val1241Ala
ENST00000650860.2:c.*1366T>C	ENSP00000498775.1:n.*1366T>C
ENST00000674945.1:c.3545T>C	ENSP00000502333.1:p.Val1182Ala
ENST00000675619.1:n.4701T>C
ENST00000675768.1:n.1089T>C
ENST00000676337.1:c.*875T>C	ENSP00000501728.1:n.*875T>C
ENST00000680586.1:n.4528T>C
ENST00000389652.9:c.3367T>C
ENST00000424120.5:c.3869T>C	ENSP00000403465.1:p.Val1290Ala
ENST00000503292.5:c.3869T>C	ENSP00000421809.1:p.Val1290Ala
ENST00000506643.4:c.2197T>C
ENST00000634028.1:c.3675T>C	ENSP00000488669.1:n.3675T>C
NM_001080522.2:c.3869T>C , LRG_697t1:c.3869T>C	NP_001073991.2:p.Val1290Ala
XM_005248177.1:c.3869T>C	XP_005248234.1:p.Val1290Ala
XM_011513869.1:c.3869T>C	XP_011512171.1:p.Val1290Ala
XM_011513870.1:c.3869T>C	XP_011512172.1:p.Val1290Ala
XM_011513871.1:c.3722T>C	XP_011512173.1:p.Val1241Ala
XM_017008482.1:c.3722T>C	XP_016863971.1:p.Val1241Ala
XR_001741296.1:n.4114T>C
NM_001378615.1:c.3869T>C MANE Select	NP_001365544.1:p.Val1290Ala
NM_001378617.1:c.3722T>C	NP_001365546.1:p.Val1241Ala