Canonical Allele Identifier: CA2637061733

Gene: ADAP2

Linked Data

• gnomAD v4: 17-30956795-C-CCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956795_30956796insCTG , CM000679.2:g.30956795_30956796insCTG	GRCh38
NC_000017.10:g.29283813_29283814insCTG , CM000679.1:g.29283813_29283814insCTG	GRCh37
NC_000017.9:g.26307939_26307940insCTG	NCBI36
NG_051975.1:g.40060_40061insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1111+326_1111+327insCTG MANE Select	ENSP00000329468.3:n.1111+326_1111+327insCTG
ENST00000330889.7:c.1111+326_1111+327insCTG	ENSP00000329468.3:n.1111+326_1111+327insCTG
ENST00000470962.1:n.531+326_531+327insCTG
ENST00000580525.5:c.1129+326_1129+327insCTG	ENSP00000464121.1:n.1129+326_1129+327insCTG
ENST00000584828.5:c.402+404_402+405insCTG
ENST00000585130.5:c.*710+326_*710+327insCTG	ENSP00000464120.1:n.*710+326_*710+327insCTG
NM_018404.2:c.1111+326_1111+327insCTG	NP_060874.1:n.1111+326_1111+327insCTG
XM_005258008.2:c.1129+326_1129+327insCTG	XP_005258065.1:n.1129+326_1129+327insCTG
XM_005258011.2:c.1066+326_1066+327insCTG	XP_005258068.1:n.1066+326_1066+327insCTG
XM_006721973.2:c.1051+404_1051+405insCTG	XP_006722036.1:n.1051+404_1051+405insCTG
XM_011524993.1:c.1126+326_1126+327insCTG	XP_011523295.1:n.1126+326_1126+327insCTG
XM_011524994.1:c.1108+326_1108+327insCTG	XP_011523296.1:n.1108+326_1108+327insCTG
NM_001346712.1:c.1129+326_1129+327insCTG	NP_001333641.1:n.1129+326_1129+327insCTG
NM_001346714.1:c.1108+326_1108+327insCTG	NP_001333643.1:n.1108+326_1108+327insCTG
NM_001346716.1:c.1033+404_1033+405insCTG	NP_001333645.1:n.1033+404_1033+405insCTG
NR_144488.1:n.1310+326_1310+327insCTG
XM_024450832.1:c.1126+326_1126+327insCTG	XP_024306600.1:n.1126+326_1126+327insCTG
XM_024450833.1:c.1066+326_1066+327insCTG	XP_024306601.1:n.1066+326_1066+327insCTG
XM_024450834.1:c.1051+404_1051+405insCTG	XP_024306602.1:n.1051+404_1051+405insCTG
XM_024450835.1:c.745+326_745+327insCTG	XP_024306603.1:n.745+326_745+327insCTG
NM_018404.3:c.1111+326_1111+327insCTG MANE Select	NP_060874.1:n.1111+326_1111+327insCTG
NM_001346712.2:c.1129+326_1129+327insCTG	NP_001333641.1:n.1129+326_1129+327insCTG
NM_001346714.2:c.1108+326_1108+327insCTG	NP_001333643.1:n.1108+326_1108+327insCTG
NM_001346716.2:c.1033+404_1033+405insCTG	NP_001333645.1:n.1033+404_1033+405insCTG
NR_144488.2:n.1101+326_1101+327insCTG