Canonical Allele Identifier: CA381550950

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257620C>T (hg19) ; chr11:g.67490149C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490149C>T , CM000673.2:g.67490149C>T	GRCh38
NC_000011.9:g.67257620C>T , CM000673.1:g.67257620C>T	GRCh37
NC_000011.8:g.67014196C>T	NCBI36
NG_008969.1:g.12116C>T , LRG_460:g.12116C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.557C>T
ENST00000528641.7:c.391C>T	ENSP00000434982.3:p.His131Tyr
ENST00000529797.2:n.1092C>T
ENST00000682324.1:c.468+694C>T	ENSP00000508017.1:n.468+694C>T
ENST00000682659.1:c.211C>T	ENSP00000507351.1:p.His71Tyr
ENST00000682699.1:c.580C>T	ENSP00000507935.1:p.His194Tyr
ENST00000683237.1:c.580C>T	ENSP00000507343.1:p.His194Tyr
ENST00000683856.1:c.403C>T	ENSP00000507979.1:p.His135Tyr
ENST00000684006.1:c.580C>T	ENSP00000507269.1:p.His194Tyr
ENST00000684657.1:c.400C>T	ENSP00000507961.1:p.His134Tyr
ENST00000279146.8:c.580C>T MANE Select	ENSP00000279146.3:p.His194Tyr
ENST00000279146.7:c.580C>T	ENSP00000279146.3:p.His194Tyr
ENST00000525341.1:c.232C>T	ENSP00000476993.1:p.His78Tyr
ENST00000528641.6:c.391C>T	ENSP00000434982.2:p.His131Tyr
NM_001302959.1:c.403C>T	NP_001289888.1:p.His135Tyr
NM_001302960.1:c.580C>T	NP_001289889.1:p.His194Tyr
NM_003977.3:c.580C>T	NP_003968.3:p.His194Tyr
XM_024448761.1:c.580C>T	XP_024304529.1:p.His194Tyr
NM_003977.4:c.580C>T MANE Select	NP_003968.3:p.His194Tyr
NM_001302960.2:c.580C>T	NP_001289889.1:p.His194Tyr
NM_001302959.2:c.403C>T	NP_001289888.1:p.His135Tyr