Canonical Allele Identifier: CA1440673398

Gene: CC2D2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.15510353_15510354delinsTG , CM000666.2:g.15510353_15510354delinsTG	GRCh38
NC_000004.11:g.15511976_15511977delinsTG , CM000666.1:g.15511976_15511977delinsTG	GRCh37
NC_000004.10:g.15121074_15121075delinsTG	NCBI36
NG_013035.1:g.45488_45489delinsTG , LRG_697:g.45488_45489delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389652.11:c.540+113_540+114delinsTG	ENSP00000374303.8:n.540+113_540+114delinsTG
ENST00000424120.6:c.540+113_540+114delinsTG MANE Select	ENSP00000403465.1:n.540+113_540+114delinsTG
ENST00000503292.6:c.540+113_540+114delinsTG	ENSP00000421809.1:n.540+113_540+114delinsTG
ENST00000506643.5:c.393+113_393+114delinsTG	ENSP00000422931.2:n.393+113_393+114delinsTG
ENST00000512702.6:c.540+113_540+114delinsTG	ENSP00000422875.2:n.540+113_540+114delinsTG
ENST00000514450.3:c.540+113_540+114delinsTG	ENSP00000502062.1:n.540+113_540+114delinsTG
ENST00000634028.2:c.393+113_393+114delinsTG	ENSP00000488669.2:n.393+113_393+114delinsTG
ENST00000650860.2:c.393+113_393+114delinsTG	ENSP00000498775.1:n.393+113_393+114delinsTG
ENST00000651385.1:c.393+113_393+114delinsTG	ENSP00000499005.1:n.393+113_393+114delinsTG
ENST00000674945.1:c.393+113_393+114delinsTG	ENSP00000502333.1:n.393+113_393+114delinsTG
ENST00000676337.1:c.393+113_393+114delinsTG	ENSP00000501728.1:n.393+113_393+114delinsTG
ENST00000424120.5:c.540+113_540+114delinsTG	ENSP00000403465.1:n.540+113_540+114delinsTG
ENST00000503292.5:c.540+113_540+114delinsTG	ENSP00000421809.1:n.540+113_540+114delinsTG
ENST00000512702.5:c.540+113_540+114delinsTG	ENSP00000422875.1:n.540+113_540+114delinsTG
ENST00000513811.5:n.720+113_720+114delinsTG
ENST00000514450.2:n.695+113_695+114delinsTG
ENST00000634028.1:c.523+113_523+114delinsTG	ENSP00000488669.1:n.523+113_523+114delinsTG
NM_001080522.2:c.540+113_540+114delinsTG , LRG_697t1:c.540+113_540+114delinsTG	NP_001073991.2:n.540+113_540+114delinsTG
XM_005248177.1:c.540+113_540+114delinsTG	XP_005248234.1:n.540+113_540+114delinsTG
XM_011513869.1:c.540+113_540+114delinsTG	XP_011512171.1:n.540+113_540+114delinsTG
XM_011513870.1:c.540+113_540+114delinsTG	XP_011512172.1:n.540+113_540+114delinsTG
XM_011513871.1:c.393+113_393+114delinsTG	XP_011512173.1:n.393+113_393+114delinsTG
XM_011513872.1:c.540+113_540+114delinsTG	XP_011512174.1:n.540+113_540+114delinsTG
XM_011513873.1:c.540+113_540+114delinsTG	XP_011512175.1:n.540+113_540+114delinsTG
XM_011513872.3:c.540+113_540+114delinsTG	XP_011512174.1:n.540+113_540+114delinsTG
XM_017008482.1:c.393+113_393+114delinsTG	XP_016863971.1:n.393+113_393+114delinsTG
XR_001741296.1:n.740+113_740+114delinsTG
NM_001378615.1:c.540+113_540+114delinsTG MANE Select	NP_001365544.1:n.540+113_540+114delinsTG
NM_001378617.1:c.393+113_393+114delinsTG	NP_001365546.1:n.393+113_393+114delinsTG