Canonical Allele Identifier: CA475392340

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67254635C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67487164C>A , CM000673.2:g.67487164C>A	GRCh38
NC_000011.9:g.67254635C>A , CM000673.1:g.67254635C>A	GRCh37
NC_000011.8:g.67011211C>A	NCBI36
NG_008969.1:g.9131C>A , LRG_460:g.9131C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.235C>A
ENST00000528641.7:c.258C>A	ENSP00000434982.3:p.Ala86=
ENST00000529797.2:n.188C>A
ENST00000682324.1:c.258C>A	ENSP00000508017.1:p.Ala86=
ENST00000682659.1:c.100-2874C>A	ENSP00000507351.1:n.100-2874C>A
ENST00000682699.1:c.258C>A	ENSP00000507935.1:p.Ala86=
ENST00000683237.1:c.258C>A	ENSP00000507343.1:p.Ala86=
ENST00000683856.1:c.81C>A	ENSP00000507979.1:p.Ala27=
ENST00000684006.1:c.258C>A	ENSP00000507269.1:p.Ala86=
ENST00000684657.1:c.100-2103C>A	ENSP00000507961.1:n.100-2103C>A
ENST00000279146.8:c.258C>A MANE Select	ENSP00000279146.3:p.Ala86=
ENST00000279146.7:c.258C>A	ENSP00000279146.3:p.Ala86=
ENST00000528641.6:c.258C>A	ENSP00000434982.2:p.Ala86=
ENST00000529797.1:n.368C>A
NM_001302959.1:c.81C>A	NP_001289888.1:p.Ala27=
NM_001302960.1:c.258C>A	NP_001289889.1:p.Ala86=
NM_003977.3:c.258C>A	NP_003968.3:p.Ala86=
XM_024448761.1:c.258C>A	XP_024304529.1:p.Ala86=
NM_003977.4:c.258C>A MANE Select	NP_003968.3:p.Ala86=
NM_001302960.2:c.258C>A	NP_001289889.1:p.Ala86=
NM_001302959.2:c.81C>A	NP_001289888.1:p.Ala27=