Canonical Allele Identifier: CA356407150

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15478762C>T , CM000666.2:g.15478762C>T	GRCh38
NC_000004.11:g.15480386C>T , CM000666.1:g.15480386C>T	GRCh37
NC_000004.10:g.15089484C>T	NCBI36
NG_013035.1:g.13898C>T , LRG_697:g.13898C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378615.1:c.79C>T MANE Select	NP_001365544.1:p.Gln27Ter
ENST00000424120.6:c.79C>T MANE Select	ENSP00000403465.1:p.Gln27Ter
NM_001080522.2:c.79C>T , LRG_697t1:c.79C>T	NP_001073991.2:p.Gln27Ter
NM_001164720.1:c.79C>T	NP_001158192.1:p.Gln27Ter
NM_001164720.2:c.79C>T	NP_001158192.1:p.Gln27Ter
NM_001164720.3:c.79C>T	NP_001158192.1:p.Gln27Ter
NM_020785.2:c.79C>T , LRG_697t2:c.79C>T	NP_065836.2:p.Gln27Ter
ENST00000389652.11:c.79C>T	ENSP00000374303.8:p.Gln27Ter
ENST00000424120.5:c.79C>T	ENSP00000403465.1:p.Gln27Ter
ENST00000438599.6:c.79C>T	ENSP00000401154.2:p.Gln27Ter
ENST00000503292.5:c.79C>T	ENSP00000421809.1:p.Gln27Ter
ENST00000503292.6:c.79C>T	ENSP00000421809.1:p.Gln27Ter
ENST00000503658.2:c.79C>T	ENSP00000426846.1:p.Gln27Ter
ENST00000507954.5:c.79C>T	ENSP00000427221.1:p.Gln27Ter
ENST00000511544.5:c.79C>T	ENSP00000426109.2:p.Gln27Ter
ENST00000511544.6:c.79C>T	ENSP00000426109.2:p.Gln27Ter
ENST00000512702.5:c.79C>T	ENSP00000422875.1:p.Gln27Ter
ENST00000512702.6:c.79C>T	ENSP00000422875.2:p.Gln27Ter
ENST00000513811.5:n.259C>T
ENST00000514450.2:n.234C>T
ENST00000514450.3:c.79C>T	ENSP00000502062.1:p.Gln27Ter
ENST00000515124.5:c.79C>T	ENSP00000424368.1:p.Gln27Ter
ENST00000515124.6:c.79C>T	ENSP00000424368.1:p.Gln27Ter
ENST00000676337.1:c.-69C>T	ENSP00000501728.1:n.-69C>T
XM_005248177.1:c.79C>T	XP_005248234.1:p.Gln27Ter
XM_011513869.1:c.79C>T	XP_011512171.1:p.Gln27Ter
XM_011513870.1:c.79C>T	XP_011512172.1:p.Gln27Ter
XM_011513872.1:c.79C>T	XP_011512174.1:p.Gln27Ter
XM_011513872.3:c.79C>T	XP_011512174.1:p.Gln27Ter
XM_011513873.1:c.79C>T	XP_011512175.1:p.Gln27Ter
XM_011513874.1:c.79C>T	XP_011512176.1:p.Gln27Ter
XM_011513874.2:c.79C>T	XP_011512176.1:p.Gln27Ter
XR_001741296.1:n.279C>T