Canonical Allele Identifier: CA381554606

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258297G>T (hg19) ; chr11:g.67490826G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490826G>T , CM000673.2:g.67490826G>T	GRCh38
NC_000011.9:g.67258297G>T , CM000673.1:g.67258297G>T	GRCh37
NC_000011.8:g.67014873G>T	NCBI36
NG_008969.1:g.12793G>T , LRG_460:g.12793G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1133G>T
ENST00000528641.7:c.637G>T	ENSP00000434982.3:p.Ala213Ser
ENST00000529797.2:n.1668G>T
ENST00000682324.1:c.469-171G>T	ENSP00000508017.1:n.469-171G>T
ENST00000682659.1:c.457G>T	ENSP00000507351.1:p.Ala153Ser
ENST00000682699.1:c.826G>T	ENSP00000507935.1:p.Ala276Ser
ENST00000683237.1:c.818G>T	ENSP00000507343.1:p.Arg273Leu
ENST00000683856.1:c.649G>T	ENSP00000507979.1:p.Ala217Ser
ENST00000684006.1:c.815G>T	ENSP00000507269.1:p.Arg272Leu
ENST00000684657.1:c.646G>T	ENSP00000507961.1:p.Ala216Ser
ENST00000279146.8:c.826G>T MANE Select	ENSP00000279146.3:p.Ala276Ser
ENST00000279146.7:c.826G>T	ENSP00000279146.3:p.Ala276Ser
ENST00000528641.6:c.637G>T	ENSP00000434982.2:p.Ala213Ser
NM_001302959.1:c.649G>T	NP_001289888.1:p.Ala217Ser
NM_001302960.1:c.818G>T	NP_001289889.1:p.Arg273Leu
NM_003977.3:c.826G>T	NP_003968.3:p.Ala276Ser
XM_024448761.1:c.826G>T	XP_024304529.1:p.Ala276Ser
NM_003977.4:c.826G>T MANE Select	NP_003968.3:p.Ala276Ser
NM_001302960.2:c.818G>T	NP_001289889.1:p.Arg273Leu
NM_001302959.2:c.649G>T	NP_001289888.1:p.Ala217Ser