Canonical Allele Identifier: CA224164630

Gene: AIP

Linked Data

• dbSNP Id: rs199777404
• gnomAD v4: 11-67489673-C-T
• MyVariant Identifiers: chr11:g.67257144C>T (hg19) ; chr11:g.67489673C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489673C>T , CM000673.2:g.67489673C>T	GRCh38
NC_000011.9:g.67257144C>T , CM000673.1:g.67257144C>T	GRCh37
NC_000011.8:g.67013720C>T	NCBI36
NG_008969.1:g.11640C>T , LRG_460:g.11640C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.445+218C>T
ENST00000528641.7:c.280-365C>T	ENSP00000434982.3:n.280-365C>T
ENST00000529797.2:n.616C>T
ENST00000682324.1:c.468+218C>T	ENSP00000508017.1:n.468+218C>T
ENST00000682659.1:c.100-365C>T	ENSP00000507351.1:n.100-365C>T
ENST00000682699.1:c.468+218C>T	ENSP00000507935.1:n.468+218C>T
ENST00000683237.1:c.468+218C>T	ENSP00000507343.1:n.468+218C>T
ENST00000683856.1:c.291+218C>T	ENSP00000507979.1:n.291+218C>T
ENST00000684006.1:c.468+218C>T	ENSP00000507269.1:n.468+218C>T
ENST00000684657.1:c.288+218C>T	ENSP00000507961.1:n.288+218C>T
ENST00000279146.8:c.468+218C>T MANE Select	ENSP00000279146.3:n.468+218C>T
ENST00000279146.7:c.468+218C>T	ENSP00000279146.3:n.468+218C>T
ENST00000525341.1:c.120+218C>T	ENSP00000476993.1:n.120+218C>T
ENST00000528641.6:c.280-365C>T	ENSP00000434982.2:n.280-365C>T
ENST00000529797.1:n.796C>T
NM_001302959.1:c.291+218C>T	NP_001289888.1:n.291+218C>T
NM_001302960.1:c.468+218C>T	NP_001289889.1:n.468+218C>T
NM_003977.3:c.468+218C>T	NP_003968.3:n.468+218C>T
XM_024448761.1:c.468+218C>T	XP_024304529.1:n.468+218C>T
NM_003977.4:c.468+218C>T MANE Select	NP_003968.3:n.468+218C>T
NM_001302960.2:c.468+218C>T	NP_001289889.1:n.468+218C>T
NM_001302959.2:c.291+218C>T	NP_001289888.1:n.291+218C>T