Canonical Allele Identifier: CA679490513

Gene: AIP

Linked Data

• dbSNP Id: rs1159484470
• gnomAD v3: 11-67483150-G-T
• gnomAD v4: 11-67483150-G-T
• MyVariant Identifiers: chr11:g.67250621G>T (hg19) ; chr11:g.67483150G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483150G>T , CM000673.2:g.67483150G>T	GRCh38
NC_000011.9:g.67250621G>T , CM000673.1:g.67250621G>T	GRCh37
NC_000011.8:g.67007197G>T	NCBI36
NG_008969.1:g.5117G>T , LRG_460:g.5117G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000528641.7:c.-9G>T	ENSP00000434982.3:n.-9G>T
ENST00000682324.1:c.-9G>T	ENSP00000508017.1:n.-9G>T
ENST00000682699.1:c.-9G>T	ENSP00000507935.1:n.-9G>T
ENST00000683237.1:c.-9G>T	ENSP00000507343.1:n.-9G>T
ENST00000684006.1:c.-9G>T	ENSP00000507269.1:n.-9G>T
ENST00000684657.1:c.-9G>T	ENSP00000507961.1:n.-9G>T
ENST00000279146.8:c.-9G>T MANE Select	ENSP00000279146.3:n.-9G>T
ENST00000279146.7:c.-9G>T	ENSP00000279146.3:n.-9G>T
ENST00000528641.6:c.-9G>T	ENSP00000434982.2:n.-9G>T
ENST00000529797.1:n.102G>T
NM_001302960.1:c.-9G>T	NP_001289889.1:n.-9G>T
NM_003977.3:c.-9G>T	NP_003968.3:n.-9G>T
XM_024448761.1:c.-9G>T	XP_024304529.1:n.-9G>T
NM_003977.4:c.-9G>T MANE Select	NP_003968.3:n.-9G>T
NM_001302960.2:c.-9G>T	NP_001289889.1:n.-9G>T