Canonical Allele Identifier: CA381554902

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258330G>T (hg19) ; chr11:g.67490859G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490859G>T , CM000673.2:g.67490859G>T	GRCh38
NC_000011.9:g.67258330G>T , CM000673.1:g.67258330G>T	GRCh37
NC_000011.8:g.67014906G>T	NCBI36
NG_008969.1:g.12826G>T , LRG_460:g.12826G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1166G>T
ENST00000528641.7:c.670G>T	ENSP00000434982.3:p.Asp224Tyr
ENST00000529797.2:n.1701G>T
ENST00000682324.1:c.469-138G>T	ENSP00000508017.1:n.469-138G>T
ENST00000682659.1:c.490G>T	ENSP00000507351.1:p.Asp164Tyr
ENST00000682699.1:c.859G>T	ENSP00000507935.1:p.Asp287Tyr
ENST00000683237.1:c.851G>T	ENSP00000507343.1:p.Ter284Leu
ENST00000683856.1:c.682G>T	ENSP00000507979.1:p.Asp228Tyr
ENST00000684006.1:c.848G>T	ENSP00000507269.1:p.Ter283Leu
ENST00000684657.1:c.679G>T	ENSP00000507961.1:p.Asp227Tyr
ENST00000279146.8:c.859G>T MANE Select	ENSP00000279146.3:p.Asp287Tyr
ENST00000279146.7:c.859G>T	ENSP00000279146.3:p.Asp287Tyr
ENST00000528641.6:c.670G>T	ENSP00000434982.2:p.Asp224Tyr
NM_001302959.1:c.682G>T	NP_001289888.1:p.Asp228Tyr
NM_001302960.1:c.851G>T	NP_001289889.1:p.Ter284Leu
NM_003977.3:c.859G>T	NP_003968.3:p.Asp287Tyr
XM_024448761.1:c.859G>T	XP_024304529.1:p.Asp287Tyr
NM_003977.4:c.859G>T MANE Select	NP_003968.3:p.Asp287Tyr
NM_001302960.2:c.851G>T	NP_001289889.1:p.Ter284Leu
NM_001302959.2:c.682G>T	NP_001289888.1:p.Asp228Tyr