Canonical Allele Identifier: CA381545757

Gene: AIP

Linked Data

• ClinVar Variation Id: 2566784
• ClinVar RCV Id: RCV003306736
• MyVariant Identifiers: chr11:g.67250660G>T (hg19) ; chr11:g.67483189G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483189G>T , CM000673.2:g.67483189G>T	GRCh38
NC_000011.9:g.67250660G>T , CM000673.1:g.67250660G>T	GRCh37
NC_000011.8:g.67007236G>T	NCBI36
NG_008969.1:g.5156G>T , LRG_460:g.5156G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.8G>T
ENST00000528641.7:c.31G>T	ENSP00000434982.3:p.Asp11Tyr
ENST00000682324.1:c.31G>T	ENSP00000508017.1:p.Asp11Tyr
ENST00000682659.1:c.31G>T	ENSP00000507351.1:p.Asp11Tyr
ENST00000682699.1:c.31G>T	ENSP00000507935.1:p.Asp11Tyr
ENST00000683237.1:c.31G>T	ENSP00000507343.1:p.Asp11Tyr
ENST00000684006.1:c.31G>T	ENSP00000507269.1:p.Asp11Tyr
ENST00000684657.1:c.31G>T	ENSP00000507961.1:p.Asp11Tyr
ENST00000279146.8:c.31G>T MANE Select	ENSP00000279146.3:p.Asp11Tyr
ENST00000279146.7:c.31G>T	ENSP00000279146.3:p.Asp11Tyr
ENST00000528641.6:c.31G>T	ENSP00000434982.2:p.Asp11Tyr
ENST00000529797.1:n.141G>T
NM_001302960.1:c.31G>T	NP_001289889.1:p.Asp11Tyr
NM_003977.3:c.31G>T	NP_003968.3:p.Asp11Tyr
XM_024448761.1:c.31G>T	XP_024304529.1:p.Asp11Tyr
NM_003977.4:c.31G>T MANE Select	NP_003968.3:p.Asp11Tyr
NM_001302960.2:c.31G>T	NP_001289889.1:p.Asp11Tyr