Canonical Allele Identifier: CA381551950

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490453C>G , CM000673.2:g.67490453C>G	GRCh38
NC_000011.9:g.67257924C>G , CM000673.1:g.67257924C>G	GRCh37
NC_000011.8:g.67014500C>G	NCBI36
NG_008969.1:g.12420C>G , LRG_460:g.12420C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003977.4:c.783C>G MANE Select	NP_003968.3:p.Tyr261Ter
ENST00000279146.8:c.783C>G MANE Select	ENSP00000279146.3:p.Tyr261Ter
NM_001302959.1:c.606C>G	NP_001289888.1:p.Tyr202Ter
NM_001302959.2:c.606C>G	NP_001289888.1:p.Tyr202Ter
NM_001302960.1:c.779+4C>G	NP_001289889.1:n.779+4C>G
NM_001302960.2:c.779+4C>G	NP_001289889.1:n.779+4C>G
NM_003977.3:c.783C>G	NP_003968.3:p.Tyr261Ter
ENST00000279146.7:c.783C>G	ENSP00000279146.3:p.Tyr261Ter
ENST00000525341.1:c.435C>G	ENSP00000476993.1:p.Tyr145Ter
ENST00000525341.2:c.760C>G
ENST00000528641.6:c.594C>G	ENSP00000434982.2:p.Tyr198Ter
ENST00000528641.7:c.594C>G	ENSP00000434982.3:p.Tyr198Ter
ENST00000529797.2:n.1295C>G
ENST00000682324.1:c.469-544C>G	ENSP00000508017.1:n.469-544C>G
ENST00000682659.1:c.414C>G	ENSP00000507351.1:p.Tyr138Ter
ENST00000682699.1:c.783C>G	ENSP00000507935.1:p.Tyr261Ter
ENST00000683237.1:c.779+4C>G	ENSP00000507343.1:n.779+4C>G
ENST00000683856.1:c.606C>G	ENSP00000507979.1:p.Tyr202Ter
ENST00000684006.1:c.783C>G	ENSP00000507269.1:p.Tyr261Ter
ENST00000684657.1:c.603C>G	ENSP00000507961.1:p.Tyr201Ter
XM_024448761.1:c.783C>G	XP_024304529.1:p.Tyr261Ter