Canonical Allele Identifier: CA356407592

Gene: CC2D2A

Linked Data

• MyVariant Identifiers: chr4:g.15482366A>G (hg19) ; chr4:g.15480742A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15480742A>G , CM000666.2:g.15480742A>G	GRCh38
NC_000004.11:g.15482366A>G , CM000666.1:g.15482366A>G	GRCh37
NC_000004.10:g.15091464A>G	NCBI36
NG_013035.1:g.15878A>G , LRG_697:g.15878A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389652.11:c.162A>G	ENSP00000374303.8:p.Lys54=
ENST00000424120.6:c.162A>G MANE Select	ENSP00000403465.1:p.Lys54=
ENST00000503292.6:c.162A>G	ENSP00000421809.1:p.Lys54=
ENST00000506643.5:c.15A>G	ENSP00000422931.2:p.Lys5=
ENST00000511544.6:c.*50A>G	ENSP00000426109.2:n.*50A>G
ENST00000512702.6:c.162A>G	ENSP00000422875.2:p.Lys54=
ENST00000514450.3:c.162A>G	ENSP00000502062.1:p.Lys54=
ENST00000515124.6:c.162A>G	ENSP00000424368.1:p.Lys54=
ENST00000634028.2:c.15A>G	ENSP00000488669.2:p.Lys5=
ENST00000650860.2:c.15A>G	ENSP00000498775.1:p.Lys5=
ENST00000651385.1:c.15A>G	ENSP00000499005.1:p.Lys5=
ENST00000652443.1:c.15A>G	ENSP00000502719.1:p.Lys5=
ENST00000674945.1:c.15A>G	ENSP00000502333.1:p.Lys5=
ENST00000676337.1:c.15A>G	ENSP00000501728.1:p.Lys5=
ENST00000424120.5:c.162A>G	ENSP00000403465.1:p.Lys54=
ENST00000438599.6:c.268A>G	ENSP00000401154.2:p.Ile90Val
ENST00000503292.5:c.162A>G	ENSP00000421809.1:p.Lys54=
ENST00000503658.2:c.268A>G	ENSP00000426846.1:p.Ile90Val
ENST00000507954.5:c.162A>G	ENSP00000427221.1:p.Lys54=
ENST00000511544.5:c.*50A>G	ENSP00000426109.2:n.*50A>G
ENST00000512702.5:c.162A>G	ENSP00000422875.1:p.Lys54=
ENST00000513811.5:n.342A>G
ENST00000514450.2:n.317A>G
ENST00000515124.5:c.162A>G	ENSP00000424368.1:p.Lys54=
ENST00000634028.1:c.145A>G	ENSP00000488669.1:p.Ile49Val
NM_001080522.2:c.162A>G , LRG_697t1:c.162A>G	NP_001073991.2:p.Lys54=
NM_001164720.1:c.162A>G	NP_001158192.1:p.Lys54=
NM_020785.2:c.268A>G , LRG_697t2:c.268A>G	NP_065836.2:p.Ile90Val
XM_005248177.1:c.162A>G	XP_005248234.1:p.Lys54=
XM_011513869.1:c.162A>G	XP_011512171.1:p.Lys54=
XM_011513870.1:c.162A>G	XP_011512172.1:p.Lys54=
XM_011513871.1:c.15A>G	XP_011512173.1:p.Lys5=
XM_011513872.1:c.162A>G	XP_011512174.1:p.Lys54=
XM_011513873.1:c.162A>G	XP_011512175.1:p.Lys54=
XM_011513874.1:c.162A>G	XP_011512176.1:p.Lys54=
XM_011513872.3:c.162A>G	XP_011512174.1:p.Lys54=
XM_011513874.2:c.162A>G	XP_011512176.1:p.Lys54=
XM_017008482.1:c.15A>G	XP_016863971.1:p.Lys5=
XR_001741296.1:n.362A>G
NM_001164720.2:c.162A>G	NP_001158192.1:p.Lys54=
NM_001164720.3:c.162A>G	NP_001158192.1:p.Lys54=
NM_001378615.1:c.162A>G MANE Select	NP_001365544.1:p.Lys54=
NM_001378617.1:c.15A>G	NP_001365546.1:p.Lys5=