Canonical Allele Identifier: CA397394613

Gene: AIPL1

Linked Data

• dbSNP Id: rs1597325600
• MyVariant Identifiers: chr17:g.6329000A>C (hg19) ; chr17:g.6425680A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425680A>C , CM000679.2:g.6425680A>C	GRCh38
NC_000017.10:g.6329000A>C , CM000679.1:g.6329000A>C	GRCh37
NC_000017.9:g.6269724A>C	NCBI36
NG_008474.1:g.14520T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381129.8:c.935T>G MANE Select	ENSP00000370521.3:p.Met312Arg
ENST00000250087.9:c.746T>G	ENSP00000250087.5:p.Met249Arg
ENST00000381128.2:c.*807T>G	ENSP00000370520.2:n.*807T>G
ENST00000381129.7:c.935T>G	ENSP00000370521.3:p.Met312Arg
ENST00000570466.5:c.869T>G	ENSP00000461287.1:p.Met290Arg
ENST00000570584.5:c.251+8239T>G
ENST00000574506.5:c.899T>G	ENSP00000458456.1:p.Met300Arg
ENST00000575265.5:c.*906T>G	ENSP00000459673.1:n.*906T>G
ENST00000576307.5:c.755T>G	ENSP00000459522.1:p.Met252Arg
ENST00000576776.5:c.863T>G	ENSP00000460827.1:p.Met288Arg
ENST00000621374.4:c.934T>G	ENSP00000481337.1:p.Trp312Gly
NM_001033054.2:c.746T>G	NP_001028226.1:p.Met249Arg
NM_001033055.2:c.755T>G	NP_001028227.1:p.Met252Arg
NM_001285399.2:c.899T>G	NP_001272328.1:p.Met300Arg
NM_001285400.2:c.869T>G	NP_001272329.1:p.Met290Arg
NM_001285401.2:c.863T>G	NP_001272330.1:p.Met288Arg
NM_001285402.1:c.818T>G	NP_001272331.1:p.Met273Arg
NM_014336.4:c.935T>G	NP_055151.3:p.Met312Arg
NM_001033054.3:c.746T>G	NP_001028226.1:p.Met249Arg
NM_001033055.3:c.755T>G	NP_001028227.1:p.Met252Arg
NM_001285399.3:c.899T>G	NP_001272328.1:p.Met300Arg
NM_001285400.3:c.869T>G	NP_001272329.1:p.Met290Arg
NM_001285401.3:c.863T>G	NP_001272330.1:p.Met288Arg
NM_001285402.2:c.818T>G	NP_001272331.1:p.Met273Arg
NM_001285403.3:c.*906T>G	NP_001272332.1:n.*906T>G
NM_014336.5:c.935T>G MANE Select	NP_055151.3:p.Met312Arg
NM_001285403.4:c.*906T>G	NP_001272332.1:n.*906T>G