Canonical Allele Identifier: CA2614623311

Gene: AIP

Linked Data

• gnomAD v4: 11-67490170-A-ATTTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490170_67490171insTTTTG , CM000673.2:g.67490170_67490171insTTTTG	GRCh38
NC_000011.9:g.67257641_67257642insTTTTG , CM000673.1:g.67257641_67257642insTTTTG	GRCh37
NC_000011.8:g.67014217_67014218insTTTTG	NCBI36
NG_008969.1:g.12137_12138insTTTTG , LRG_460:g.12137_12138insTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.578_579insTTTTG
ENST00000528641.7:c.412_413insTTTTG	ENSP00000434982.3:p.Lys138IlefsTer16
ENST00000529797.2:n.1113_1114insTTTTG
ENST00000682324.1:c.468+715_468+716insTTTTG	ENSP00000508017.1:n.468+715_468+716insTTTTG
ENST00000682659.1:c.232_233insTTTTG	ENSP00000507351.1:p.Lys78IlefsTer16
ENST00000682699.1:c.601_602insTTTTG	ENSP00000507935.1:p.Lys201IlefsTer16
ENST00000683237.1:c.601_602insTTTTG	ENSP00000507343.1:p.Lys201IlefsTer16
ENST00000683856.1:c.424_425insTTTTG	ENSP00000507979.1:p.Lys142IlefsTer16
ENST00000684006.1:c.601_602insTTTTG	ENSP00000507269.1:p.Lys201IlefsTer16
ENST00000684657.1:c.421_422insTTTTG	ENSP00000507961.1:p.Lys141IlefsTer16
ENST00000279146.8:c.601_602insTTTTG MANE Select	ENSP00000279146.3:p.Lys201IlefsTer16
ENST00000279146.7:c.601_602insTTTTG	ENSP00000279146.3:p.Lys201IlefsTer16
ENST00000525341.1:c.253_254insTTTTG	ENSP00000476993.1:p.Lys85IlefsTer16
ENST00000528641.6:c.412_413insTTTTG	ENSP00000434982.2:p.Lys138IlefsTer16
NM_001302959.1:c.424_425insTTTTG	NP_001289888.1:p.Lys142IlefsTer16
NM_001302960.1:c.601_602insTTTTG	NP_001289889.1:p.Lys201IlefsTer16
NM_003977.3:c.601_602insTTTTG	NP_003968.3:p.Lys201IlefsTer16
XM_024448761.1:c.601_602insTTTTG	XP_024304529.1:p.Lys201IlefsTer16
NM_003977.4:c.601_602insTTTTG MANE Select	NP_003968.3:p.Lys201IlefsTer16
NM_001302960.2:c.601_602insTTTTG	NP_001289889.1:p.Lys201IlefsTer16
NM_001302959.2:c.424_425insTTTTG	NP_001289888.1:p.Lys142IlefsTer16