Canonical Allele Identifier: CA6140938

Gene: AIP

Linked Data

• ClinVar Variation Id: 1107627
• ClinVar RCV Id: RCV001432846
• dbSNP Id: rs749392143
• ExAC: 11:67257937 C / T
• gnomAD v2: 11-67257937-C-T
• gnomAD v3: 11-67490466-C-T
• gnomAD v4: 11-67490466-C-T
• MyVariant Identifiers: chr11:g.67257937C>T (hg19) ; chr11:g.67490466C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490466C>T , CM000673.2:g.67490466C>T	GRCh38
NC_000011.9:g.67257937C>T , CM000673.1:g.67257937C>T	GRCh37
NC_000011.8:g.67014513C>T	NCBI36
NG_008969.1:g.12433C>T , LRG_460:g.12433C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.773C>T
ENST00000528641.7:c.598+9C>T	ENSP00000434982.3:n.598+9C>T
ENST00000529797.2:n.1308C>T
ENST00000682324.1:c.469-531C>T	ENSP00000508017.1:n.469-531C>T
ENST00000682659.1:c.418+9C>T	ENSP00000507351.1:n.418+9C>T
ENST00000682699.1:c.787+9C>T	ENSP00000507935.1:n.787+9C>T
ENST00000683237.1:c.779+17C>T	ENSP00000507343.1:n.779+17C>T
ENST00000683856.1:c.610+9C>T	ENSP00000507979.1:n.610+9C>T
ENST00000684006.1:c.787+9C>T	ENSP00000507269.1:n.787+9C>T
ENST00000684657.1:c.607+9C>T	ENSP00000507961.1:n.607+9C>T
ENST00000279146.8:c.787+9C>T MANE Select	ENSP00000279146.3:n.787+9C>T
ENST00000279146.7:c.787+9C>T	ENSP00000279146.3:n.787+9C>T
ENST00000525341.1:c.448C>T	ENSP00000476993.1:p.Arg150Trp
ENST00000528641.6:c.598+9C>T	ENSP00000434982.2:n.598+9C>T
NM_001302959.1:c.610+9C>T	NP_001289888.1:n.610+9C>T
NM_001302960.1:c.779+17C>T	NP_001289889.1:n.779+17C>T
NM_003977.3:c.787+9C>T	NP_003968.3:n.787+9C>T
XM_024448761.1:c.787+9C>T	XP_024304529.1:n.787+9C>T
NM_003977.4:c.787+9C>T MANE Select	NP_003968.3:n.787+9C>T
NM_001302960.2:c.779+17C>T	NP_001289889.1:n.779+17C>T
NM_001302959.2:c.610+9C>T	NP_001289888.1:n.610+9C>T