Canonical Allele Identifier: CA3703979

Gene: FLOT1

Linked Data

• dbSNP Id: rs10947089
• ExAC: 6:30710135 A / G
• gnomAD v2: 6-30710135-A-G
• gnomAD v3: 6-30742358-A-G
• gnomAD v4: 6-30742358-A-G
• MyVariant Identifiers: chr6:g.30710135A>G (hg19) ; chr6:g.30742358A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30742358A>G , CM000668.2:g.30742358A>G	GRCh38
NC_000006.11:g.30710135A>G , CM000668.1:g.30710135A>G	GRCh37
NC_000006.10:g.30818114A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376389.8:c.-14-155T>C MANE Select	ENSP00000365569.3:n.-14-155T>C
ENST00000376389.7:c.-14-155T>C	ENSP00000365569.3:n.-14-155T>C
ENST00000438162.5:c.-15+26T>C	ENSP00000400615.1:n.-15+26T>C
ENST00000454845.1:c.-15+109T>C	ENSP00000391341.1:n.-15+109T>C
ENST00000470643.5:n.207-155T>C
ENST00000484168.1:n.181-155T>C
ENST00000484693.1:n.152-155T>C
NM_005803.2:c.-14-155T>C	NP_005794.1:n.-14-155T>C
XM_005248780.3:c.-15+109T>C	XP_005248837.1:n.-15+109T>C
XM_005248781.3:c.-14-155T>C	XP_005248838.1:n.-14-155T>C
XM_006714947.2:c.-14-155T>C	XP_006715010.1:n.-14-155T>C
NM_001318875.1:c.-14-155T>C	NP_001305804.1:n.-14-155T>C
NM_005803.3:c.-14-155T>C	NP_005794.1:n.-14-155T>C
XM_006714947.3:c.-14-155T>C	XP_006715010.1:n.-14-155T>C
XM_017010157.1:c.42+109T>C	XP_016865646.1:n.42+109T>C
XM_017010158.1:c.42+109T>C	XP_016865647.1:n.42+109T>C
NM_005803.4:c.-14-155T>C MANE Select	NP_005794.1:n.-14-155T>C
NM_001318875.2:c.-14-155T>C	NP_001305804.1:n.-14-155T>C