Canonical Allele Identifier: CA2614625359

Gene: AIP

Linked Data

• gnomAD v4: 11-67490677-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490677G>T , CM000673.2:g.67490677G>T	GRCh38
NC_000011.9:g.67258148G>T , CM000673.1:g.67258148G>T	GRCh37
NC_000011.8:g.67014724G>T	NCBI36
NG_008969.1:g.12644G>T , LRG_460:g.12644G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.984G>T
ENST00000528641.7:c.599-111G>T	ENSP00000434982.3:n.599-111G>T
ENST00000529797.2:n.1519G>T
ENST00000682324.1:c.469-320G>T	ENSP00000508017.1:n.469-320G>T
ENST00000682659.1:c.419-111G>T	ENSP00000507351.1:n.419-111G>T
ENST00000682699.1:c.788-111G>T	ENSP00000507935.1:n.788-111G>T
ENST00000683237.1:c.780-111G>T	ENSP00000507343.1:n.780-111G>T
ENST00000683856.1:c.611-111G>T	ENSP00000507979.1:n.611-111G>T
ENST00000684006.1:c.788-122G>T	ENSP00000507269.1:n.788-122G>T
ENST00000684657.1:c.608-111G>T	ENSP00000507961.1:n.608-111G>T
ENST00000279146.8:c.788-111G>T MANE Select	ENSP00000279146.3:n.788-111G>T
ENST00000279146.7:c.788-111G>T	ENSP00000279146.3:n.788-111G>T
ENST00000528641.6:c.599-111G>T	ENSP00000434982.2:n.599-111G>T
NM_001302959.1:c.611-111G>T	NP_001289888.1:n.611-111G>T
NM_001302960.1:c.780-111G>T	NP_001289889.1:n.780-111G>T
NM_003977.3:c.788-111G>T	NP_003968.3:n.788-111G>T
XM_024448761.1:c.788-111G>T	XP_024304529.1:n.788-111G>T
NM_003977.4:c.788-111G>T MANE Select	NP_003968.3:n.788-111G>T
NM_001302960.2:c.780-111G>T	NP_001289889.1:n.780-111G>T
NM_001302959.2:c.611-111G>T	NP_001289888.1:n.611-111G>T