Canonical Allele Identifier: CA421236760

Gene: FLAD1

Linked Data

• MyVariant Identifiers: chr1:g.154965230G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154992754G>C , CM000663.2:g.154992754G>C	GRCh38
NC_000001.10:g.154965230G>C , CM000663.1:g.154965230G>C	GRCh37
NC_000001.9:g.153231854G>C	NCBI36
NG_042310.1:g.14461G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000292180.8:c.1596G>C MANE Select	ENSP00000292180.3:p.Leu532=
ENST00000292180.7:c.1596G>C	ENSP00000292180.3:p.Leu532=
ENST00000295530.6:c.*11+81G>C	ENSP00000295530.2:n.*11+81G>C
ENST00000315144.14:c.1305G>C	ENSP00000317296.10:p.Leu435=
ENST00000368428.1:c.219G>C	ENSP00000357413.1:p.Leu73=
ENST00000368432.5:c.1305G>C	ENSP00000357417.1:p.Leu435=
ENST00000477609.5:n.344+81G>C
ENST00000481758.1:n.166G>C
ENST00000489992.5:n.406G>C
NM_001184891.1:c.1305G>C	NP_001171820.1:p.Leu435=
NM_025207.4:c.1596G>C	NP_079483.3:p.Leu532=
NM_201398.2:c.1305G>C	NP_958800.1:p.Leu435=
XM_005245503.2:c.795G>C	XP_005245560.1:p.Leu265=
XR_241098.3:n.1366G>C
NM_025207.5:c.1596G>C MANE Select	NP_079483.3:p.Leu532=
NM_001184891.2:c.1305G>C	NP_001171820.1:p.Leu435=
NM_201398.3:c.1305G>C	NP_958800.1:p.Leu435=