Canonical Allele Identifier: CA381549430

Gene: AIP

Linked Data

• COSMIC: COSM1193977
• MyVariant Identifiers: chr11:g.67256838T>A (hg19) ; chr11:g.67489367T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67489367T>A , CM000673.2:g.67489367T>A	GRCh38
NC_000011.9:g.67256838T>A , CM000673.1:g.67256838T>A	GRCh37
NC_000011.8:g.67013414T>A	NCBI36
NG_008969.1:g.11334T>A , LRG_460:g.11334T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.357T>A
ENST00000528641.7:c.280-671T>A	ENSP00000434982.3:n.280-671T>A
ENST00000529797.2:n.310T>A
ENST00000682324.1:c.380T>A	ENSP00000508017.1:p.Met127Lys
ENST00000682659.1:c.100-671T>A	ENSP00000507351.1:n.100-671T>A
ENST00000682699.1:c.380T>A	ENSP00000507935.1:p.Met127Lys
ENST00000683237.1:c.380T>A	ENSP00000507343.1:p.Met127Lys
ENST00000683856.1:c.203T>A	ENSP00000507979.1:p.Met68Lys
ENST00000684006.1:c.380T>A	ENSP00000507269.1:p.Met127Lys
ENST00000684657.1:c.200T>A	ENSP00000507961.1:p.Met67Lys
ENST00000279146.8:c.380T>A MANE Select	ENSP00000279146.3:p.Met127Lys
ENST00000279146.7:c.380T>A	ENSP00000279146.3:p.Met127Lys
ENST00000525341.1:c.32T>A	ENSP00000476993.1:p.Met11Lys
ENST00000528641.6:c.280-671T>A	ENSP00000434982.2:n.280-671T>A
ENST00000529797.1:n.490T>A
NM_001302959.1:c.203T>A	NP_001289888.1:p.Met68Lys
NM_001302960.1:c.380T>A	NP_001289889.1:p.Met127Lys
NM_003977.3:c.380T>A	NP_003968.3:p.Met127Lys
XM_024448761.1:c.380T>A	XP_024304529.1:p.Met127Lys
NM_003977.4:c.380T>A MANE Select	NP_003968.3:p.Met127Lys
NM_001302960.2:c.380T>A	NP_001289889.1:p.Met127Lys
NM_001302959.2:c.203T>A	NP_001289888.1:p.Met68Lys