Canonical Allele Identifier: CA475509152

Gene: AIP

Linked Data

• gnomAD v4: 11-67490789-C-T
• MyVariant Identifiers: chr11:g.67258260C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490789C>T , CM000673.2:g.67490789C>T	GRCh38
NC_000011.9:g.67258260C>T , CM000673.1:g.67258260C>T	GRCh37
NC_000011.8:g.67014836C>T	NCBI36
NG_008969.1:g.12756C>T , LRG_460:g.12756C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1096C>T
ENST00000528641.7:c.600C>T	ENSP00000434982.3:p.Asp200=
ENST00000529797.2:n.1631C>T
ENST00000682324.1:c.469-208C>T	ENSP00000508017.1:n.469-208C>T
ENST00000682659.1:c.420C>T	ENSP00000507351.1:p.Asp140=
ENST00000682699.1:c.789C>T	ENSP00000507935.1:p.Asp263=
ENST00000683237.1:c.781C>T	ENSP00000507343.1:p.Gln261Ter
ENST00000683856.1:c.612C>T	ENSP00000507979.1:p.Asp204=
ENST00000684006.1:c.788-10C>T	ENSP00000507269.1:n.788-10C>T
ENST00000684657.1:c.609C>T	ENSP00000507961.1:p.Asp203=
ENST00000279146.8:c.789C>T MANE Select	ENSP00000279146.3:p.Asp263=
ENST00000279146.7:c.789C>T	ENSP00000279146.3:p.Asp263=
ENST00000528641.6:c.600C>T	ENSP00000434982.2:p.Asp200=
NM_001302959.1:c.612C>T	NP_001289888.1:p.Asp204=
NM_001302960.1:c.781C>T	NP_001289889.1:p.Gln261Ter
NM_003977.3:c.789C>T	NP_003968.3:p.Asp263=
XM_024448761.1:c.789C>T	XP_024304529.1:p.Asp263=
NM_003977.4:c.789C>T MANE Select	NP_003968.3:p.Asp263=
NM_001302960.2:c.781C>T	NP_001289889.1:p.Gln261Ter
NM_001302959.2:c.612C>T	NP_001289888.1:p.Asp204=