Canonical Allele Identifier: CA381551971

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257933G>C (hg19) ; chr11:g.67490462G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490462G>C , CM000673.2:g.67490462G>C	GRCh38
NC_000011.9:g.67257933G>C , CM000673.1:g.67257933G>C	GRCh37
NC_000011.8:g.67014509G>C	NCBI36
NG_008969.1:g.12429G>C , LRG_460:g.12429G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.769G>C
ENST00000528641.7:c.598+5G>C	ENSP00000434982.3:n.598+5G>C
ENST00000529797.2:n.1304G>C
ENST00000682324.1:c.469-535G>C	ENSP00000508017.1:n.469-535G>C
ENST00000682659.1:c.418+5G>C	ENSP00000507351.1:n.418+5G>C
ENST00000682699.1:c.787+5G>C	ENSP00000507935.1:n.787+5G>C
ENST00000683237.1:c.779+13G>C	ENSP00000507343.1:n.779+13G>C
ENST00000683856.1:c.610+5G>C	ENSP00000507979.1:n.610+5G>C
ENST00000684006.1:c.787+5G>C	ENSP00000507269.1:n.787+5G>C
ENST00000684657.1:c.607+5G>C	ENSP00000507961.1:n.607+5G>C
ENST00000279146.8:c.787+5G>C MANE Select	ENSP00000279146.3:n.787+5G>C
ENST00000279146.7:c.787+5G>C	ENSP00000279146.3:n.787+5G>C
ENST00000525341.1:c.444G>C	ENSP00000476993.1:p.Glu148Asp
ENST00000528641.6:c.598+5G>C	ENSP00000434982.2:n.598+5G>C
NM_001302959.1:c.610+5G>C	NP_001289888.1:n.610+5G>C
NM_001302960.1:c.779+13G>C	NP_001289889.1:n.779+13G>C
NM_003977.3:c.787+5G>C	NP_003968.3:n.787+5G>C
XM_024448761.1:c.787+5G>C	XP_024304529.1:n.787+5G>C
NM_003977.4:c.787+5G>C MANE Select	NP_003968.3:n.787+5G>C
NM_001302960.2:c.779+13G>C	NP_001289889.1:n.779+13G>C
NM_001302959.2:c.610+5G>C	NP_001289888.1:n.610+5G>C