Canonical Allele Identifier: CA475509217

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257619G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490148G>C , CM000673.2:g.67490148G>C	GRCh38
NC_000011.9:g.67257619G>C , CM000673.1:g.67257619G>C	GRCh37
NC_000011.8:g.67014195G>C	NCBI36
NG_008969.1:g.12115G>C , LRG_460:g.12115G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.556G>C
ENST00000528641.7:c.390G>C	ENSP00000434982.3:p.Gly130=
ENST00000529797.2:n.1091G>C
ENST00000682324.1:c.468+693G>C	ENSP00000508017.1:n.468+693G>C
ENST00000682659.1:c.210G>C	ENSP00000507351.1:p.Gly70=
ENST00000682699.1:c.579G>C	ENSP00000507935.1:p.Gly193=
ENST00000683237.1:c.579G>C	ENSP00000507343.1:p.Gly193=
ENST00000683856.1:c.402G>C	ENSP00000507979.1:p.Gly134=
ENST00000684006.1:c.579G>C	ENSP00000507269.1:p.Gly193=
ENST00000684657.1:c.399G>C	ENSP00000507961.1:p.Gly133=
ENST00000279146.8:c.579G>C MANE Select	ENSP00000279146.3:p.Gly193=
ENST00000279146.7:c.579G>C	ENSP00000279146.3:p.Gly193=
ENST00000525341.1:c.231G>C	ENSP00000476993.1:p.Gly77=
ENST00000528641.6:c.390G>C	ENSP00000434982.2:p.Gly130=
NM_001302959.1:c.402G>C	NP_001289888.1:p.Gly134=
NM_001302960.1:c.579G>C	NP_001289889.1:p.Gly193=
NM_003977.3:c.579G>C	NP_003968.3:p.Gly193=
XM_024448761.1:c.579G>C	XP_024304529.1:p.Gly193=
NM_003977.4:c.579G>C MANE Select	NP_003968.3:p.Gly193=
NM_001302960.2:c.579G>C	NP_001289889.1:p.Gly193=
NM_001302959.2:c.402G>C	NP_001289888.1:p.Gly134=