Canonical Allele Identifier: CA403137655

Gene: PNPLA6

Linked Data

• MyVariant Identifiers: chr19:g.7625592T>C (hg19) ; chr19:g.7560706T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7560706T>C , CM000681.2:g.7560706T>C	GRCh38
NC_000019.9:g.7625592T>C , CM000681.1:g.7625592T>C	GRCh37
NC_000019.8:g.7531592T>C	NCBI36
NG_013374.1:g.31555T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600737.6:c.3758T>C MANE Select	ENSP00000473211.1:p.Ile1253Thr
ENST00000221249.10:c.3644T>C	ENSP00000221249.5:p.Ile1215Thr
ENST00000414982.7:c.3788T>C	ENSP00000407509.2:p.Ile1263Thr
ENST00000450331.7:c.3644T>C	ENSP00000394348.2:p.Ile1215Thr
ENST00000545201.6:c.3563T>C	ENSP00000443323.1:p.Ile1188Thr
ENST00000597202.1:n.116T>C
ENST00000599947.1:c.186-308T>C
ENST00000600737.5:c.3758T>C	ENSP00000473211.1:p.Ile1253Thr
NM_001166111.1:c.3788T>C	NP_001159583.1:p.Ile1263Thr
NM_001166112.1:c.3563T>C	NP_001159584.1:p.Ile1188Thr
NM_001166113.1:c.3644T>C	NP_001159585.1:p.Ile1215Thr
NM_001166114.1:c.3758T>C	NP_001159586.1:p.Ile1253Thr
NM_006702.4:c.3644T>C	NP_006693.3:p.Ile1215Thr
NM_001166111.2:c.3788T>C	NP_001159583.1:p.Ile1263Thr
NM_001166114.2:c.3758T>C MANE Select	NP_001159586.1:p.Ile1253Thr
NM_006702.5:c.3644T>C	NP_006693.3:p.Ile1215Thr
NM_001166112.2:c.3563T>C	NP_001159584.1:p.Ile1188Thr