Canonical Allele Identifier: CA381555016

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258341A>T (hg19) ; chr11:g.67490870A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490870A>T , CM000673.2:g.67490870A>T	GRCh38
NC_000011.9:g.67258341A>T , CM000673.1:g.67258341A>T	GRCh37
NC_000011.8:g.67014917A>T	NCBI36
NG_008969.1:g.12837A>T , LRG_460:g.12837A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1177A>T
ENST00000528641.7:c.681A>T	ENSP00000434982.3:p.Lys227Asn
ENST00000529797.2:n.1712A>T
ENST00000682324.1:c.469-127A>T	ENSP00000508017.1:n.469-127A>T
ENST00000682659.1:c.501A>T	ENSP00000507351.1:p.Lys167Asn
ENST00000682699.1:c.870A>T	ENSP00000507935.1:p.Lys290Asn
ENST00000683237.1:c.*10A>T	ENSP00000507343.1:n.*10A>T
ENST00000683856.1:c.693A>T	ENSP00000507979.1:p.Lys231Asn
ENST00000684006.1:c.*10A>T	ENSP00000507269.1:n.*10A>T
ENST00000684657.1:c.690A>T	ENSP00000507961.1:p.Lys230Asn
ENST00000279146.8:c.870A>T MANE Select	ENSP00000279146.3:p.Lys290Asn
ENST00000279146.7:c.870A>T	ENSP00000279146.3:p.Lys290Asn
ENST00000528641.6:c.681A>T	ENSP00000434982.2:p.Lys227Asn
NM_001302959.1:c.693A>T	NP_001289888.1:p.Lys231Asn
NM_001302960.1:c.*10A>T	NP_001289889.1:n.*10A>T
NM_003977.3:c.870A>T	NP_003968.3:p.Lys290Asn
XM_024448761.1:c.870A>T	XP_024304529.1:p.Lys290Asn
NM_003977.4:c.870A>T MANE Select	NP_003968.3:p.Lys290Asn
NM_001302960.2:c.*10A>T	NP_001289889.1:n.*10A>T
NM_001302959.2:c.693A>T	NP_001289888.1:p.Lys231Asn