Canonical Allele Identifier: CA497687468

Gene: AIPL1

Linked Data

• MyVariant Identifiers: chr17:g.6329011C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6425691C>G , CM000679.2:g.6425691C>G	GRCh38
NC_000017.10:g.6329011C>G , CM000679.1:g.6329011C>G	GRCh37
NC_000017.9:g.6269735C>G	NCBI36
NG_008474.1:g.14509G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000381129.8:c.924G>C MANE Select	ENSP00000370521.3:p.Leu308=
ENST00000250087.9:c.735G>C	ENSP00000250087.5:p.Leu245=
ENST00000381128.2:c.*796G>C	ENSP00000370520.2:n.*796G>C
ENST00000381129.7:c.924G>C	ENSP00000370521.3:p.Leu308=
ENST00000570466.5:c.858G>C	ENSP00000461287.1:p.Leu286=
ENST00000570584.5:c.251+8228G>C
ENST00000574506.5:c.888G>C	ENSP00000458456.1:p.Leu296=
ENST00000575265.5:c.*895G>C	ENSP00000459673.1:n.*895G>C
ENST00000576307.5:c.744G>C	ENSP00000459522.1:p.Leu248=
ENST00000576776.5:c.852G>C	ENSP00000460827.1:p.Leu284=
ENST00000621374.4:c.924G>C	ENSP00000481337.1:p.Leu308=
NM_001033054.2:c.735G>C	NP_001028226.1:p.Leu245=
NM_001033055.2:c.744G>C	NP_001028227.1:p.Leu248=
NM_001285399.2:c.888G>C	NP_001272328.1:p.Leu296=
NM_001285400.2:c.858G>C	NP_001272329.1:p.Leu286=
NM_001285401.2:c.852G>C	NP_001272330.1:p.Leu284=
NM_001285402.1:c.807G>C	NP_001272331.1:p.Leu269=
NM_014336.4:c.924G>C	NP_055151.3:p.Leu308=
NM_001033054.3:c.735G>C	NP_001028226.1:p.Leu245=
NM_001033055.3:c.744G>C	NP_001028227.1:p.Leu248=
NM_001285399.3:c.888G>C	NP_001272328.1:p.Leu296=
NM_001285400.3:c.858G>C	NP_001272329.1:p.Leu286=
NM_001285401.3:c.852G>C	NP_001272330.1:p.Leu284=
NM_001285402.2:c.807G>C	NP_001272331.1:p.Leu269=
NM_001285403.3:c.*895G>C	NP_001272332.1:n.*895G>C
NM_014336.5:c.924G>C MANE Select	NP_055151.3:p.Leu308=
NM_001285403.4:c.*895G>C	NP_001272332.1:n.*895G>C