Canonical Allele Identifier: CA1980172498

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490498_67490500delinsCAG , CM000673.2:g.67490498_67490500delinsCAG	GRCh38
NC_000011.9:g.67257969_67257971delinsCAG , CM000673.1:g.67257969_67257971delinsCAG	GRCh37
NC_000011.8:g.67014545_67014547delinsCAG	NCBI36
NG_008969.1:g.12465_12467delinsCAG , LRG_460:g.12465_12467delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.805_807delinsCAG
ENST00000528641.7:c.598+41_598+43delinsCAG	ENSP00000434982.3:n.598+41_598+43delinsCAG
ENST00000529797.2:n.1340_1342delinsCAG
ENST00000682324.1:c.469-499_469-497delinsCAG	ENSP00000508017.1:n.469-499_469-497delinsCAG
ENST00000682659.1:c.418+41_418+43delinsCAG	ENSP00000507351.1:n.418+41_418+43delinsCAG
ENST00000682699.1:c.787+41_787+43delinsCAG	ENSP00000507935.1:n.787+41_787+43delinsCAG
ENST00000683237.1:c.779+49_779+51delinsCAG	ENSP00000507343.1:n.779+49_779+51delinsCAG
ENST00000683856.1:c.610+41_610+43delinsCAG	ENSP00000507979.1:n.610+41_610+43delinsCAG
ENST00000684006.1:c.787+41_787+43delinsCAG	ENSP00000507269.1:n.787+41_787+43delinsCAG
ENST00000684657.1:c.607+41_607+43delinsCAG	ENSP00000507961.1:n.607+41_607+43delinsCAG
ENST00000279146.8:c.787+41_787+43delinsCAG MANE Select	ENSP00000279146.3:n.787+41_787+43delinsCAG
ENST00000279146.7:c.787+41_787+43delinsCAG	ENSP00000279146.3:n.787+41_787+43delinsCAG
ENST00000525341.1:c.480_482delinsCAG	ENSP00000476993.1:p.Val160=
ENST00000528641.6:c.598+41_598+43delinsCAG	ENSP00000434982.2:n.598+41_598+43delinsCAG
NM_001302959.1:c.610+41_610+43delinsCAG	NP_001289888.1:n.610+41_610+43delinsCAG
NM_001302960.1:c.779+49_779+51delinsCAG	NP_001289889.1:n.779+49_779+51delinsCAG
NM_003977.3:c.787+41_787+43delinsCAG	NP_003968.3:n.787+41_787+43delinsCAG
XM_024448761.1:c.787+41_787+43delinsCAG	XP_024304529.1:n.787+41_787+43delinsCAG
NM_003977.4:c.787+41_787+43delinsCAG MANE Select	NP_003968.3:n.787+41_787+43delinsCAG
NM_001302960.2:c.779+49_779+51delinsCAG	NP_001289889.1:n.779+49_779+51delinsCAG
NM_001302959.2:c.610+41_610+43delinsCAG	NP_001289888.1:n.610+41_610+43delinsCAG