Canonical Allele Identifier: CA381551704

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257850T>A (hg19) ; chr11:g.67490379T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490379T>A , CM000673.2:g.67490379T>A	GRCh38
NC_000011.9:g.67257850T>A , CM000673.1:g.67257850T>A	GRCh37
NC_000011.8:g.67014426T>A	NCBI36
NG_008969.1:g.12346T>A , LRG_460:g.12346T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.686T>A
ENST00000528641.7:c.520T>A	ENSP00000434982.3:p.Tyr174Asn
ENST00000529797.2:n.1221T>A
ENST00000682324.1:c.469-618T>A	ENSP00000508017.1:n.469-618T>A
ENST00000682659.1:c.340T>A	ENSP00000507351.1:p.Tyr114Asn
ENST00000682699.1:c.709T>A	ENSP00000507935.1:p.Tyr237Asn
ENST00000683237.1:c.709T>A	ENSP00000507343.1:p.Tyr237Asn
ENST00000683856.1:c.532T>A	ENSP00000507979.1:p.Tyr178Asn
ENST00000684006.1:c.709T>A	ENSP00000507269.1:p.Tyr237Asn
ENST00000684657.1:c.529T>A	ENSP00000507961.1:p.Tyr177Asn
ENST00000279146.8:c.709T>A MANE Select	ENSP00000279146.3:p.Tyr237Asn
ENST00000279146.7:c.709T>A	ENSP00000279146.3:p.Tyr237Asn
ENST00000525341.1:c.361T>A	ENSP00000476993.1:p.Tyr121Asn
ENST00000528641.6:c.520T>A	ENSP00000434982.2:p.Tyr174Asn
NM_001302959.1:c.532T>A	NP_001289888.1:p.Tyr178Asn
NM_001302960.1:c.709T>A	NP_001289889.1:p.Tyr237Asn
NM_003977.3:c.709T>A	NP_003968.3:p.Tyr237Asn
XM_024448761.1:c.709T>A	XP_024304529.1:p.Tyr237Asn
NM_003977.4:c.709T>A MANE Select	NP_003968.3:p.Tyr237Asn
NM_001302960.2:c.709T>A	NP_001289889.1:p.Tyr237Asn
NM_001302959.2:c.532T>A	NP_001289888.1:p.Tyr178Asn