Canonical Allele Identifier: CA381550734

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67257588A>C (hg19) ; chr11:g.67490117A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490117A>C , CM000673.2:g.67490117A>C	GRCh38
NC_000011.9:g.67257588A>C , CM000673.1:g.67257588A>C	GRCh37
NC_000011.8:g.67014164A>C	NCBI36
NG_008969.1:g.12084A>C , LRG_460:g.12084A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525341.2:c.525A>C
ENST00000528641.7:c.359A>C	ENSP00000434982.3:p.His120Pro
ENST00000529797.2:n.1060A>C
ENST00000682324.1:c.468+662A>C	ENSP00000508017.1:n.468+662A>C
ENST00000682659.1:c.179A>C	ENSP00000507351.1:p.His60Pro
ENST00000682699.1:c.548A>C	ENSP00000507935.1:p.His183Pro
ENST00000683237.1:c.548A>C	ENSP00000507343.1:p.His183Pro
ENST00000683856.1:c.371A>C	ENSP00000507979.1:p.His124Pro
ENST00000684006.1:c.548A>C	ENSP00000507269.1:p.His183Pro
ENST00000684657.1:c.368A>C	ENSP00000507961.1:p.His123Pro
ENST00000279146.8:c.548A>C MANE Select	ENSP00000279146.3:p.His183Pro
ENST00000279146.7:c.548A>C	ENSP00000279146.3:p.His183Pro
ENST00000525341.1:c.200A>C	ENSP00000476993.1:p.His67Pro
ENST00000528641.6:c.359A>C	ENSP00000434982.2:p.His120Pro
NM_001302959.1:c.371A>C	NP_001289888.1:p.His124Pro
NM_001302960.1:c.548A>C	NP_001289889.1:p.His183Pro
NM_003977.3:c.548A>C	NP_003968.3:p.His183Pro
XM_024448761.1:c.548A>C	XP_024304529.1:p.His183Pro
NM_003977.4:c.548A>C MANE Select	NP_003968.3:p.His183Pro
NM_001302960.2:c.548A>C	NP_001289889.1:p.His183Pro
NM_001302959.2:c.371A>C	NP_001289888.1:p.His124Pro