Canonical Allele Identifier: CA2614627593

Gene: AIP

Linked Data

• gnomAD v4: 11-67491048-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67491048C>G , CM000673.2:g.67491048C>G	GRCh38
NC_000011.9:g.67258519C>G , CM000673.1:g.67258519C>G	GRCh37
NC_000011.8:g.67015095C>G	NCBI36
NG_008969.1:g.13015C>G , LRG_460:g.13015C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528641.7:c.*55C>G	ENSP00000434982.3:n.*55C>G
ENST00000529797.2:n.1890C>G
ENST00000682324.1:c.520C>G	ENSP00000508017.1:p.Pro174Ala
ENST00000682659.1:c.*55C>G	ENSP00000507351.1:n.*55C>G
ENST00000683237.1:c.*188C>G	ENSP00000507343.1:n.*188C>G
ENST00000683856.1:c.*55C>G	ENSP00000507979.1:n.*55C>G
ENST00000684006.1:c.*188C>G	ENSP00000507269.1:n.*188C>G
ENST00000684657.1:c.*55C>G	ENSP00000507961.1:n.*55C>G
ENST00000279146.8:c.*55C>G MANE Select	ENSP00000279146.3:n.*55C>G
ENST00000279146.7:c.*55C>G	ENSP00000279146.3:n.*55C>G
NM_001302959.1:c.*55C>G	NP_001289888.1:n.*55C>G
NM_001302960.1:c.*188C>G	NP_001289889.1:n.*188C>G
NM_003977.3:c.*55C>G	NP_003968.3:n.*55C>G
XM_024448761.1:c.*55C>G	XP_024304529.1:n.*55C>G
NM_003977.4:c.*55C>G MANE Select	NP_003968.3:n.*55C>G
NM_001302960.2:c.*188C>G	NP_001289889.1:n.*188C>G
NM_001302959.2:c.*55C>G	NP_001289888.1:n.*55C>G