Canonical Allele Identifier: CA2695214799

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67487146_67487147delinsTG , CM000673.2:g.67487146_67487147delinsTG	GRCh38
NC_000011.9:g.67254617_67254618delinsTG , CM000673.1:g.67254617_67254618delinsTG	GRCh37
NC_000011.8:g.67011193_67011194delinsTG	NCBI36
NG_008969.1:g.9113_9114delinsTG , LRG_460:g.9113_9114delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.217_218delinsTG
ENST00000528641.7:c.240_241delinsTG	ENSP00000434982.3:p.Met80_Arg81delinsIleGly
ENST00000529797.2:n.170_171delinsTG
ENST00000682324.1:c.240_241delinsTG	ENSP00000508017.1:p.Met80_Arg81delinsIleGly
ENST00000682659.1:c.100-2892_100-2891delinsTG	ENSP00000507351.1:n.100-2892_100-2891delinsTG
ENST00000682699.1:c.240_241delinsTG	ENSP00000507935.1:p.Met80_Arg81delinsIleGly
ENST00000683237.1:c.240_241delinsTG	ENSP00000507343.1:p.Met80_Arg81delinsIleGly
ENST00000683856.1:c.63_64delinsTG	ENSP00000507979.1:p.Met21_Arg22delinsIleGly
ENST00000684006.1:c.240_241delinsTG	ENSP00000507269.1:p.Met80_Arg81delinsIleGly
ENST00000684657.1:c.100-2121_100-2120delinsTG	ENSP00000507961.1:n.100-2121_100-2120delinsTG
ENST00000279146.8:c.240_241delinsTG MANE Select	ENSP00000279146.3:p.Met80_Arg81delinsIleGly
ENST00000279146.7:c.240_241delinsTG	ENSP00000279146.3:p.Met80_Arg81delinsIleGly
ENST00000528641.6:c.240_241delinsTG	ENSP00000434982.2:p.Met80_Arg81delinsIleGly
ENST00000529797.1:n.350_351delinsTG
NM_001302959.1:c.63_64delinsTG	NP_001289888.1:p.Met21_Arg22delinsIleGly
NM_001302960.1:c.240_241delinsTG	NP_001289889.1:p.Met80_Arg81delinsIleGly
NM_003977.3:c.240_241delinsTG	NP_003968.3:p.Met80_Arg81delinsIleGly
XM_024448761.1:c.240_241delinsTG	XP_024304529.1:p.Met80_Arg81delinsIleGly
NM_003977.4:c.240_241delinsTG MANE Select	NP_003968.3:p.Met80_Arg81delinsIleGly
NM_001302960.2:c.240_241delinsTG	NP_001289889.1:p.Met80_Arg81delinsIleGly
NM_001302959.2:c.63_64delinsTG	NP_001289888.1:p.Met21_Arg22delinsIleGly