Canonical Allele Identifier: CA381550889

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257608T>G (hg19) ; chr11:g.67490137T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490137T>G , CM000673.2:g.67490137T>G	GRCh38
NC_000011.9:g.67257608T>G , CM000673.1:g.67257608T>G	GRCh37
NC_000011.8:g.67014184T>G	NCBI36
NG_008969.1:g.12104T>G , LRG_460:g.12104T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.545T>G
ENST00000528641.7:c.379T>G	ENSP00000434982.3:p.Tyr127Asp
ENST00000529797.2:n.1080T>G
ENST00000682324.1:c.468+682T>G	ENSP00000508017.1:n.468+682T>G
ENST00000682659.1:c.199T>G	ENSP00000507351.1:p.Tyr67Asp
ENST00000682699.1:c.568T>G	ENSP00000507935.1:p.Tyr190Asp
ENST00000683237.1:c.568T>G	ENSP00000507343.1:p.Tyr190Asp
ENST00000683856.1:c.391T>G	ENSP00000507979.1:p.Tyr131Asp
ENST00000684006.1:c.568T>G	ENSP00000507269.1:p.Tyr190Asp
ENST00000684657.1:c.388T>G	ENSP00000507961.1:p.Tyr130Asp
ENST00000279146.8:c.568T>G MANE Select	ENSP00000279146.3:p.Tyr190Asp
ENST00000279146.7:c.568T>G	ENSP00000279146.3:p.Tyr190Asp
ENST00000525341.1:c.220T>G	ENSP00000476993.1:p.Tyr74Asp
ENST00000528641.6:c.379T>G	ENSP00000434982.2:p.Tyr127Asp
NM_001302959.1:c.391T>G	NP_001289888.1:p.Tyr131Asp
NM_001302960.1:c.568T>G	NP_001289889.1:p.Tyr190Asp
NM_003977.3:c.568T>G	NP_003968.3:p.Tyr190Asp
XM_024448761.1:c.568T>G	XP_024304529.1:p.Tyr190Asp
NM_003977.4:c.568T>G MANE Select	NP_003968.3:p.Tyr190Asp
NM_001302960.2:c.568T>G	NP_001289889.1:p.Tyr190Asp
NM_001302959.2:c.391T>G	NP_001289888.1:p.Tyr131Asp