Canonical Allele Identifier: CA7813030

Gene: IFT140

Linked Data

• dbSNP Id: rs779007169
• ExAC: 16:1570178 C / G
• gnomAD v2: 16-1570178-C-G
• gnomAD v4: 16-1520177-C-G
• MyVariant Identifiers: chr16:g.1570178C>G (hg19) ; chr16:g.1520177C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1520177C>G , CM000678.2:g.1520177C>G	GRCh38
NC_000016.9:g.1570178C>G , CM000678.1:g.1570178C>G	GRCh37
NC_000016.8:g.1510179C>G	NCBI36
NG_032783.1:g.96932G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3827G>C MANE Select	ENSP00000406012.2:p.Gly1276Ala
ENST00000361339.9:c.1409G>C	ENSP00000354895.5:p.Gly470Ala
ENST00000397417.6:c.*2265G>C	ENSP00000380562.2:n.*2265G>C
ENST00000426508.6:c.3827G>C	ENSP00000406012.2:p.Gly1276Ala
ENST00000565298.5:n.3651G>C
NM_014714.3:c.3827G>C	NP_055529.2:p.Gly1276Ala
XM_006720989.2:c.3827G>C	XP_006721052.1:p.Gly1276Ala
XM_006720990.2:c.3827G>C	XP_006721053.1:p.Gly1276Ala
XM_006720991.2:c.3827G>C	XP_006721054.1:p.Gly1276Ala
XM_006720992.2:c.1460G>C	XP_006721055.1:p.Gly487Ala
XM_011522766.1:c.3581G>C	XP_011521068.1:p.Gly1194Ala
XM_011522767.1:c.2852G>C	XP_011521069.1:p.Gly951Ala
XM_006720990.3:c.3827G>C	XP_006721053.1:p.Gly1276Ala
XM_006720991.3:c.3827G>C	XP_006721054.1:p.Gly1276Ala
XM_006720992.3:c.1460G>C	XP_006721055.1:p.Gly487Ala
XM_011522766.3:c.3581G>C	XP_011521068.1:p.Gly1194Ala
XM_011522767.2:c.2852G>C	XP_011521069.1:p.Gly951Ala
XM_017023910.1:c.3827G>C	XP_016879399.1:p.Gly1276Ala
XM_017023911.1:c.2012G>C	XP_016879400.1:p.Gly671Ala
NM_014714.4:c.3827G>C MANE Select	NP_055529.2:p.Gly1276Ala