Canonical Allele Identifier: CA2574896179

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67483141G>T , CM000673.2:g.67483141G>T	GRCh38
NC_000011.9:g.67250612G>T , CM000673.1:g.67250612G>T	GRCh37
NC_000011.8:g.67007188G>T	NCBI36
NG_008969.1:g.5108G>T , LRG_460:g.5108G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000528641.7:c.-18G>T	ENSP00000434982.3:n.-18G>T
ENST00000682324.1:c.-18G>T	ENSP00000508017.1:n.-18G>T
ENST00000682699.1:c.-18G>T	ENSP00000507935.1:n.-18G>T
ENST00000683237.1:c.-18G>T	ENSP00000507343.1:n.-18G>T
ENST00000684006.1:c.-18G>T	ENSP00000507269.1:n.-18G>T
ENST00000684657.1:c.-18G>T	ENSP00000507961.1:n.-18G>T
ENST00000279146.8:c.-18G>T MANE Select	ENSP00000279146.3:n.-18G>T
ENST00000279146.7:c.-18G>T	ENSP00000279146.3:n.-18G>T
ENST00000528641.6:c.-18G>T	ENSP00000434982.2:n.-18G>T
ENST00000529797.1:n.93G>T
NM_001302960.1:c.-18G>T	NP_001289889.1:n.-18G>T
NM_003977.3:c.-18G>T	NP_003968.3:n.-18G>T
XM_024448761.1:c.-18G>T	XP_024304529.1:n.-18G>T
NM_003977.4:c.-18G>T MANE Select	NP_003968.3:n.-18G>T
NM_001302960.2:c.-18G>T	NP_001289889.1:n.-18G>T