Canonical Allele Identifier: CA381554974

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258336G>T (hg19) ; chr11:g.67490865G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490865G>T , CM000673.2:g.67490865G>T	GRCh38
NC_000011.9:g.67258336G>T , CM000673.1:g.67258336G>T	GRCh37
NC_000011.8:g.67014912G>T	NCBI36
NG_008969.1:g.12832G>T , LRG_460:g.12832G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1172G>T
ENST00000528641.7:c.676G>T	ENSP00000434982.3:p.Ala226Ser
ENST00000529797.2:n.1707G>T
ENST00000682324.1:c.469-132G>T	ENSP00000508017.1:n.469-132G>T
ENST00000682659.1:c.496G>T	ENSP00000507351.1:p.Ala166Ser
ENST00000682699.1:c.865G>T	ENSP00000507935.1:p.Ala289Ser
ENST00000683237.1:c.*5G>T	ENSP00000507343.1:n.*5G>T
ENST00000683856.1:c.688G>T	ENSP00000507979.1:p.Ala230Ser
ENST00000684006.1:c.*5G>T	ENSP00000507269.1:n.*5G>T
ENST00000684657.1:c.685G>T	ENSP00000507961.1:p.Ala229Ser
ENST00000279146.8:c.865G>T MANE Select	ENSP00000279146.3:p.Ala289Ser
ENST00000279146.7:c.865G>T	ENSP00000279146.3:p.Ala289Ser
ENST00000528641.6:c.676G>T	ENSP00000434982.2:p.Ala226Ser
NM_001302959.1:c.688G>T	NP_001289888.1:p.Ala230Ser
NM_001302960.1:c.*5G>T	NP_001289889.1:n.*5G>T
NM_003977.3:c.865G>T	NP_003968.3:p.Ala289Ser
XM_024448761.1:c.865G>T	XP_024304529.1:p.Ala289Ser
NM_003977.4:c.865G>T MANE Select	NP_003968.3:p.Ala289Ser
NM_001302960.2:c.*5G>T	NP_001289889.1:n.*5G>T
NM_001302959.2:c.688G>T	NP_001289888.1:p.Ala230Ser