Canonical Allele Identifier: CA486191964

Gene: ATL1

Linked Data

• MyVariant Identifiers: chr14:g.51094868T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50628150T>C , CM000676.2:g.50628150T>C	GRCh38
NC_000014.8:g.51094868T>C , CM000676.1:g.51094868T>C	GRCh37
NC_000014.7:g.50164618T>C	NCBI36
NG_009028.1:g.100069T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553509.2:c.1239T>C	ENSP00000450989.2:p.Phe413=
ENST00000556478.3:c.1239T>C	ENSP00000501428.2:p.Phe413=
ENST00000682037.1:c.1239T>C	ENSP00000508289.1:p.Phe413=
ENST00000682219.1:n.2577T>C
ENST00000683037.1:n.1160T>C
ENST00000683330.1:n.1573T>C
ENST00000358385.12:c.1239T>C MANE Select	ENSP00000351155.7:p.Phe413=
ENST00000674288.1:c.*2531T>C	ENSP00000501522.1:n.*2531T>C
ENST00000358385.10:c.1239T>C	ENSP00000351155.6:p.Phe413=
ENST00000441560.6:c.1239T>C	ENSP00000413675.2:p.Phe413=
ENST00000555266.1:c.382T>C	ENSP00000450897.1:n.382T>C
NM_001127713.1:c.1239T>C	NP_001121185.1:p.Phe413=
NM_015915.4:c.1239T>C	NP_056999.2:p.Phe413=
NM_181598.3:c.1239T>C	NP_853629.2:p.Phe413=
NM_015915.5:c.1239T>C MANE Select	NP_056999.2:p.Phe413=
NM_181598.4:c.1239T>C	NP_853629.2:p.Phe413=