Canonical Allele Identifier: CA1980172740

Gene: AIP

Linked Data

• dbSNP Id: rs1865899996
• gnomAD v4: 11-67490999-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490999G>A , CM000673.2:g.67490999G>A	GRCh38
NC_000011.9:g.67258470G>A , CM000673.1:g.67258470G>A	GRCh37
NC_000011.8:g.67015046G>A	NCBI36
NG_008969.1:g.12966G>A , LRG_460:g.12966G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000528641.7:c.*6G>A	ENSP00000434982.3:n.*6G>A
ENST00000529797.2:n.1841G>A
ENST00000682324.1:c.471G>A	ENSP00000508017.1:p.Glu157=
ENST00000682659.1:c.*6G>A	ENSP00000507351.1:n.*6G>A
ENST00000683237.1:c.*139G>A	ENSP00000507343.1:n.*139G>A
ENST00000683856.1:c.*6G>A	ENSP00000507979.1:n.*6G>A
ENST00000684006.1:c.*139G>A	ENSP00000507269.1:n.*139G>A
ENST00000684657.1:c.*6G>A	ENSP00000507961.1:n.*6G>A
ENST00000279146.8:c.*6G>A MANE Select	ENSP00000279146.3:n.*6G>A
ENST00000279146.7:c.*6G>A	ENSP00000279146.3:n.*6G>A
NM_001302959.1:c.*6G>A	NP_001289888.1:n.*6G>A
NM_001302960.1:c.*139G>A	NP_001289889.1:n.*139G>A
NM_003977.3:c.*6G>A	NP_003968.3:n.*6G>A
XM_024448761.1:c.*6G>A	XP_024304529.1:n.*6G>A
NM_003977.4:c.*6G>A MANE Select	NP_003968.3:n.*6G>A
NM_001302960.2:c.*139G>A	NP_001289889.1:n.*139G>A
NM_001302959.2:c.*6G>A	NP_001289888.1:n.*6G>A