Canonical Allele Identifier: CA381554561

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258295A>C (hg19) ; chr11:g.67490824A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490824A>C , CM000673.2:g.67490824A>C	GRCh38
NC_000011.9:g.67258295A>C , CM000673.1:g.67258295A>C	GRCh37
NC_000011.8:g.67014871A>C	NCBI36
NG_008969.1:g.12791A>C , LRG_460:g.12791A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.1131A>C
ENST00000528641.7:c.635A>C	ENSP00000434982.3:p.His212Pro
ENST00000529797.2:n.1666A>C
ENST00000682324.1:c.469-173A>C	ENSP00000508017.1:n.469-173A>C
ENST00000682659.1:c.455A>C	ENSP00000507351.1:p.His152Pro
ENST00000682699.1:c.824A>C	ENSP00000507935.1:p.His275Pro
ENST00000683237.1:c.816A>C	ENSP00000507343.1:p.Pro272=
ENST00000683856.1:c.647A>C	ENSP00000507979.1:p.His216Pro
ENST00000684006.1:c.813A>C	ENSP00000507269.1:p.Pro271=
ENST00000684657.1:c.644A>C	ENSP00000507961.1:p.His215Pro
ENST00000279146.8:c.824A>C MANE Select	ENSP00000279146.3:p.His275Pro
ENST00000279146.7:c.824A>C	ENSP00000279146.3:p.His275Pro
ENST00000528641.6:c.635A>C	ENSP00000434982.2:p.His212Pro
NM_001302959.1:c.647A>C	NP_001289888.1:p.His216Pro
NM_001302960.1:c.816A>C	NP_001289889.1:p.Pro272=
NM_003977.3:c.824A>C	NP_003968.3:p.His275Pro
XM_024448761.1:c.824A>C	XP_024304529.1:p.His275Pro
NM_003977.4:c.824A>C MANE Select	NP_003968.3:p.His275Pro
NM_001302960.2:c.816A>C	NP_001289889.1:p.Pro272=
NM_001302959.2:c.647A>C	NP_001289888.1:p.His216Pro