Canonical Allele Identifier: CA397394647

Gene: AIPL1

Linked Data

• MyVariant Identifiers: chr17:g.6329013G>C (hg19) ; chr17:g.6425693G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425693G>C , CM000679.2:g.6425693G>C	GRCh38
NC_000017.10:g.6329013G>C , CM000679.1:g.6329013G>C	GRCh37
NC_000017.9:g.6269737G>C	NCBI36
NG_008474.1:g.14507C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.922C>G MANE Select	ENSP00000370521.3:p.Leu308Val
ENST00000250087.9:c.733C>G	ENSP00000250087.5:p.Leu245Val
ENST00000381128.2:c.*794C>G	ENSP00000370520.2:n.*794C>G
ENST00000381129.7:c.922C>G	ENSP00000370521.3:p.Leu308Val
ENST00000570466.5:c.856C>G	ENSP00000461287.1:p.Leu286Val
ENST00000570584.5:c.251+8226C>G
ENST00000574506.5:c.886C>G	ENSP00000458456.1:p.Leu296Val
ENST00000575265.5:c.*893C>G	ENSP00000459673.1:n.*893C>G
ENST00000576307.5:c.742C>G	ENSP00000459522.1:p.Leu248Val
ENST00000576776.5:c.850C>G	ENSP00000460827.1:p.Leu284Val
ENST00000621374.4:c.922C>G	ENSP00000481337.1:p.Leu308Val
NM_001033054.2:c.733C>G	NP_001028226.1:p.Leu245Val
NM_001033055.2:c.742C>G	NP_001028227.1:p.Leu248Val
NM_001285399.2:c.886C>G	NP_001272328.1:p.Leu296Val
NM_001285400.2:c.856C>G	NP_001272329.1:p.Leu286Val
NM_001285401.2:c.850C>G	NP_001272330.1:p.Leu284Val
NM_001285402.1:c.805C>G	NP_001272331.1:p.Leu269Val
NM_014336.4:c.922C>G	NP_055151.3:p.Leu308Val
NM_001033054.3:c.733C>G	NP_001028226.1:p.Leu245Val
NM_001033055.3:c.742C>G	NP_001028227.1:p.Leu248Val
NM_001285399.3:c.886C>G	NP_001272328.1:p.Leu296Val
NM_001285400.3:c.856C>G	NP_001272329.1:p.Leu286Val
NM_001285401.3:c.850C>G	NP_001272330.1:p.Leu284Val
NM_001285402.2:c.805C>G	NP_001272331.1:p.Leu269Val
NM_001285403.3:c.*893C>G	NP_001272332.1:n.*893C>G
NM_014336.5:c.922C>G MANE Select	NP_055151.3:p.Leu308Val
NM_001285403.4:c.*893C>G	NP_001272332.1:n.*893C>G