Canonical Allele Identifier: CA1980172570

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490641G= , CM000673.2:g.67490641G=	GRCh38
NC_000011.9:g.67258112G= , CM000673.1:g.67258112G=	GRCh37
NC_000011.8:g.67014688G=	NCBI36
NG_008969.1:g.12608G= , LRG_460:g.12608G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.948G=
ENST00000528641.7:c.599-147G=	ENSP00000434982.3:n.599-147G=
ENST00000529797.2:n.1483G=
ENST00000682324.1:c.469-356G=	ENSP00000508017.1:n.469-356G=
ENST00000682659.1:c.419-147G=	ENSP00000507351.1:n.419-147G=
ENST00000682699.1:c.788-147G=	ENSP00000507935.1:n.788-147G=
ENST00000683237.1:c.780-147G=	ENSP00000507343.1:n.780-147G=
ENST00000683856.1:c.611-147G=	ENSP00000507979.1:n.611-147G=
ENST00000684006.1:c.788-158G=	ENSP00000507269.1:n.788-158G=
ENST00000684657.1:c.608-147G=	ENSP00000507961.1:n.608-147G=
ENST00000279146.8:c.788-147G= MANE Select	ENSP00000279146.3:n.788-147G=
ENST00000279146.7:c.788-147G=	ENSP00000279146.3:n.788-147G=
ENST00000525341.1:c.623G=	ENSP00000476993.1:n.623G=
ENST00000528641.6:c.599-147G=	ENSP00000434982.2:n.599-147G=
NM_001302959.1:c.611-147G=	NP_001289888.1:n.611-147G=
NM_001302960.1:c.780-147G=	NP_001289889.1:n.780-147G=
NM_003977.3:c.788-147G=	NP_003968.3:n.788-147G=
XM_024448761.1:c.788-147G=	XP_024304529.1:n.788-147G=
NM_003977.4:c.788-147G= MANE Select	NP_003968.3:n.788-147G=
NM_001302960.2:c.780-147G=	NP_001289889.1:n.780-147G=
NM_001302959.2:c.611-147G=	NP_001289888.1:n.611-147G=