Canonical Allele Identifier: CA381550807

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257596G>T (hg19) ; chr11:g.67490125G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490125G>T , CM000673.2:g.67490125G>T	GRCh38
NC_000011.9:g.67257596G>T , CM000673.1:g.67257596G>T	GRCh37
NC_000011.8:g.67014172G>T	NCBI36
NG_008969.1:g.12092G>T , LRG_460:g.12092G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.533G>T
ENST00000528641.7:c.367G>T	ENSP00000434982.3:p.Gly123Cys
ENST00000529797.2:n.1068G>T
ENST00000682324.1:c.468+670G>T	ENSP00000508017.1:n.468+670G>T
ENST00000682659.1:c.187G>T	ENSP00000507351.1:p.Gly63Cys
ENST00000682699.1:c.556G>T	ENSP00000507935.1:p.Gly186Cys
ENST00000683237.1:c.556G>T	ENSP00000507343.1:p.Gly186Cys
ENST00000683856.1:c.379G>T	ENSP00000507979.1:p.Gly127Cys
ENST00000684006.1:c.556G>T	ENSP00000507269.1:p.Gly186Cys
ENST00000684657.1:c.376G>T	ENSP00000507961.1:p.Gly126Cys
ENST00000279146.8:c.556G>T MANE Select	ENSP00000279146.3:p.Gly186Cys
ENST00000279146.7:c.556G>T	ENSP00000279146.3:p.Gly186Cys
ENST00000525341.1:c.208G>T	ENSP00000476993.1:p.Gly70Cys
ENST00000528641.6:c.367G>T	ENSP00000434982.2:p.Gly123Cys
NM_001302959.1:c.379G>T	NP_001289888.1:p.Gly127Cys
NM_001302960.1:c.556G>T	NP_001289889.1:p.Gly186Cys
NM_003977.3:c.556G>T	NP_003968.3:p.Gly186Cys
XM_024448761.1:c.556G>T	XP_024304529.1:p.Gly186Cys
NM_003977.4:c.556G>T MANE Select	NP_003968.3:p.Gly186Cys
NM_001302960.2:c.556G>T	NP_001289889.1:p.Gly186Cys
NM_001302959.2:c.379G>T	NP_001289888.1:p.Gly127Cys