Canonical Allele Identifier: CA381550594

Gene: AIP

Linked Data

• gnomAD v4: 11-67490093-A-T
• MyVariant Identifiers: chr11:g.67257564A>T (hg19) ; chr11:g.67490093A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490093A>T , CM000673.2:g.67490093A>T	GRCh38
NC_000011.9:g.67257564A>T , CM000673.1:g.67257564A>T	GRCh37
NC_000011.8:g.67014140A>T	NCBI36
NG_008969.1:g.12060A>T , LRG_460:g.12060A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.501A>T
ENST00000528641.7:c.335A>T	ENSP00000434982.3:p.Lys112Met
ENST00000529797.2:n.1036A>T
ENST00000682324.1:c.468+638A>T	ENSP00000508017.1:n.468+638A>T
ENST00000682659.1:c.155A>T	ENSP00000507351.1:p.Lys52Met
ENST00000682699.1:c.524A>T	ENSP00000507935.1:p.Lys175Met
ENST00000683237.1:c.524A>T	ENSP00000507343.1:p.Lys175Met
ENST00000683856.1:c.347A>T	ENSP00000507979.1:p.Lys116Met
ENST00000684006.1:c.524A>T	ENSP00000507269.1:p.Lys175Met
ENST00000684657.1:c.344A>T	ENSP00000507961.1:p.Lys115Met
ENST00000279146.8:c.524A>T MANE Select	ENSP00000279146.3:p.Lys175Met
ENST00000279146.7:c.524A>T	ENSP00000279146.3:p.Lys175Met
ENST00000525341.1:c.176A>T	ENSP00000476993.1:p.Lys59Met
ENST00000528641.6:c.335A>T	ENSP00000434982.2:p.Lys112Met
NM_001302959.1:c.347A>T	NP_001289888.1:p.Lys116Met
NM_001302960.1:c.524A>T	NP_001289889.1:p.Lys175Met
NM_003977.3:c.524A>T	NP_003968.3:p.Lys175Met
XM_024448761.1:c.524A>T	XP_024304529.1:p.Lys175Met
NM_003977.4:c.524A>T MANE Select	NP_003968.3:p.Lys175Met
NM_001302960.2:c.524A>T	NP_001289889.1:p.Lys175Met
NM_001302959.2:c.347A>T	NP_001289888.1:p.Lys116Met