Canonical Allele Identifier: CA381551986

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257936C>G (hg19) ; chr11:g.67490465C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490465C>G , CM000673.2:g.67490465C>G	GRCh38
NC_000011.9:g.67257936C>G , CM000673.1:g.67257936C>G	GRCh37
NC_000011.8:g.67014512C>G	NCBI36
NG_008969.1:g.12432C>G , LRG_460:g.12432C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.772C>G
ENST00000528641.7:c.598+8C>G	ENSP00000434982.3:n.598+8C>G
ENST00000529797.2:n.1307C>G
ENST00000682324.1:c.469-532C>G	ENSP00000508017.1:n.469-532C>G
ENST00000682659.1:c.418+8C>G	ENSP00000507351.1:n.418+8C>G
ENST00000682699.1:c.787+8C>G	ENSP00000507935.1:n.787+8C>G
ENST00000683237.1:c.779+16C>G	ENSP00000507343.1:n.779+16C>G
ENST00000683856.1:c.610+8C>G	ENSP00000507979.1:n.610+8C>G
ENST00000684006.1:c.787+8C>G	ENSP00000507269.1:n.787+8C>G
ENST00000684657.1:c.607+8C>G	ENSP00000507961.1:n.607+8C>G
ENST00000279146.8:c.787+8C>G MANE Select	ENSP00000279146.3:n.787+8C>G
ENST00000279146.7:c.787+8C>G	ENSP00000279146.3:n.787+8C>G
ENST00000525341.1:c.447C>G	ENSP00000476993.1:p.His149Gln
ENST00000528641.6:c.598+8C>G	ENSP00000434982.2:n.598+8C>G
NM_001302959.1:c.610+8C>G	NP_001289888.1:n.610+8C>G
NM_001302960.1:c.779+16C>G	NP_001289889.1:n.779+16C>G
NM_003977.3:c.787+8C>G	NP_003968.3:n.787+8C>G
XM_024448761.1:c.787+8C>G	XP_024304529.1:n.787+8C>G
NM_003977.4:c.787+8C>G MANE Select	NP_003968.3:n.787+8C>G
NM_001302960.2:c.779+16C>G	NP_001289889.1:n.779+16C>G
NM_001302959.2:c.610+8C>G	NP_001289888.1:n.610+8C>G