Canonical Allele Identifier: CA486353540

Gene: ATL1

Linked Data

• MyVariant Identifiers: chr14:g.51054610A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50587892A>C , CM000676.2:g.50587892A>C	GRCh38
NC_000014.8:g.51054610A>C , CM000676.1:g.51054610A>C	GRCh37
NC_000014.7:g.50124360A>C	NCBI36
NG_009028.1:g.59811A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000553509.2:c.96A>C	ENSP00000450989.2:p.Ala32=
ENST00000553746.2:n.297A>C
ENST00000556478.3:c.96A>C	ENSP00000501428.2:p.Ala32=
ENST00000682037.1:c.96A>C	ENSP00000508289.1:p.Ala32=
ENST00000682219.1:n.975A>C
ENST00000682226.1:n.430A>C
ENST00000682487.1:n.430A>C
ENST00000683330.1:n.430A>C
ENST00000683703.1:n.430A>C
ENST00000683837.1:n.430A>C
ENST00000684737.1:n.430A>C
ENST00000358385.12:c.96A>C MANE Select	ENSP00000351155.7:p.Ala32=
ENST00000674288.1:c.96A>C	ENSP00000501522.1:p.Ala32=
ENST00000674478.1:n.430A>C
ENST00000674503.1:c.-154A>C	ENSP00000501520.1:n.-154A>C
ENST00000358385.10:c.96A>C	ENSP00000351155.6:p.Ala32=
ENST00000441560.6:c.96A>C	ENSP00000413675.2:p.Ala32=
ENST00000554886.1:c.-150-3049A>C	ENSP00000452074.1:n.-150-3049A>C
ENST00000555960.5:c.96A>C	ENSP00000452506.1:p.Ala32=
ENST00000556478.2:n.600A>C
ENST00000557735.1:c.-154A>C	ENSP00000451015.1:n.-154A>C
NM_001127713.1:c.96A>C	NP_001121185.1:p.Ala32=
NM_015915.4:c.96A>C	NP_056999.2:p.Ala32=
NM_181598.3:c.96A>C	NP_853629.2:p.Ala32=
NM_015915.5:c.96A>C MANE Select	NP_056999.2:p.Ala32=
NM_181598.4:c.96A>C	NP_853629.2:p.Ala32=