Canonical Allele Identifier: CA2863967
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 429980
dbSNP Id: rs200904521
gnomAD v2: 4-15556832-C-T
gnomAD v3: 4-15555209-C-T
gnomAD v4: 4-15555209-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.15555209C>T , CM000666.2:g.15555209C>T GRCh38
NC_000004.11:g.15556832C>T , CM000666.1:g.15556832C>T GRCh37
NC_000004.10:g.15165930C>T NCBI36
NG_013035.1:g.90344C>T , LRG_697:g.90344C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389652.11:c.2624C>T ENSP00000374303.8:p.Ser875Leu
ENST00000424120.6:c.2624C>T MANE Select ENSP00000403465.1:p.Ser875Leu
ENST00000503292.6:c.2624C>T ENSP00000421809.1:p.Ser875Leu
ENST00000506643.5:c.2477C>T ENSP00000422931.2:p.Ser826Leu
ENST00000634028.2:c.2477C>T ENSP00000488669.2:p.Ser826Leu
ENST00000650860.2:c.2477C>T ENSP00000498775.1:p.Ser826Leu
ENST00000674945.1:c.2477C>T ENSP00000502333.1:p.Ser826Leu
ENST00000675619.1:n.703C>T
ENST00000676337.1:c.2477C>T ENSP00000501728.1:p.Ser826Leu
ENST00000680586.1:n.551C>T
ENST00000389652.9:c.2086C>T
ENST00000424120.5:c.2624C>T ENSP00000403465.1:p.Ser875Leu
ENST00000503292.5:c.2624C>T ENSP00000421809.1:p.Ser875Leu
ENST00000506643.4:c.952C>T
ENST00000512202.1:n.529C>T
ENST00000634028.1:c.2607C>T ENSP00000488669.1:n.2607C>T
NM_001080522.2:c.2624C>T , LRG_697t1:c.2624C>T NP_001073991.2:p.Ser875Leu
XM_005248177.1:c.2624C>T XP_005248234.1:p.Ser875Leu
XM_011513869.1:c.2624C>T XP_011512171.1:p.Ser875Leu
XM_011513870.1:c.2624C>T XP_011512172.1:p.Ser875Leu
XM_011513871.1:c.2477C>T XP_011512173.1:p.Ser826Leu
XM_011513872.1:c.2624C>T XP_011512174.1:p.Ser875Leu
XM_011513873.1:c.2624C>T XP_011512175.1:p.Ser875Leu
XM_011513872.3:c.2624C>T XP_011512174.1:p.Ser875Leu
XM_017008482.1:c.2477C>T XP_016863971.1:p.Ser826Leu
XR_001741296.1:n.2824C>T
NM_001378615.1:c.2624C>T MANE Select NP_001365544.1:p.Ser875Leu
NM_001378617.1:c.2477C>T NP_001365546.1:p.Ser826Leu