Canonical Allele Identifier: CA381551001

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257628G>T (hg19) ; chr11:g.67490157G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490157G>T , CM000673.2:g.67490157G>T	GRCh38
NC_000011.9:g.67257628G>T , CM000673.1:g.67257628G>T	GRCh37
NC_000011.8:g.67014204G>T	NCBI36
NG_008969.1:g.12124G>T , LRG_460:g.12124G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.565G>T
ENST00000528641.7:c.399G>T	ENSP00000434982.3:p.Lys133Asn
ENST00000529797.2:n.1100G>T
ENST00000682324.1:c.468+702G>T	ENSP00000508017.1:n.468+702G>T
ENST00000682659.1:c.219G>T	ENSP00000507351.1:p.Lys73Asn
ENST00000682699.1:c.588G>T	ENSP00000507935.1:p.Lys196Asn
ENST00000683237.1:c.588G>T	ENSP00000507343.1:p.Lys196Asn
ENST00000683856.1:c.411G>T	ENSP00000507979.1:p.Lys137Asn
ENST00000684006.1:c.588G>T	ENSP00000507269.1:p.Lys196Asn
ENST00000684657.1:c.408G>T	ENSP00000507961.1:p.Lys136Asn
ENST00000279146.8:c.588G>T MANE Select	ENSP00000279146.3:p.Lys196Asn
ENST00000279146.7:c.588G>T	ENSP00000279146.3:p.Lys196Asn
ENST00000525341.1:c.240G>T	ENSP00000476993.1:p.Lys80Asn
ENST00000528641.6:c.399G>T	ENSP00000434982.2:p.Lys133Asn
NM_001302959.1:c.411G>T	NP_001289888.1:p.Lys137Asn
NM_001302960.1:c.588G>T	NP_001289889.1:p.Lys196Asn
NM_003977.3:c.588G>T	NP_003968.3:p.Lys196Asn
XM_024448761.1:c.588G>T	XP_024304529.1:p.Lys196Asn
NM_003977.4:c.588G>T MANE Select	NP_003968.3:p.Lys196Asn
NM_001302960.2:c.588G>T	NP_001289889.1:p.Lys196Asn
NM_001302959.2:c.411G>T	NP_001289888.1:p.Lys137Asn