Canonical Allele Identifier: CA7814382

Gene: IFT140

Linked Data

• dbSNP Id: rs754001291
• ExAC: 16:1634311 G / C
• gnomAD v2: 16-1634311-G-C
• gnomAD v4: 16-1584310-G-C
• MyVariant Identifiers: chr16:g.1634311G>C (hg19) ; chr16:g.1584310G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1584310G>C , CM000678.2:g.1584310G>C	GRCh38
NC_000016.9:g.1634311G>C , CM000678.1:g.1634311G>C	GRCh37
NC_000016.8:g.1574312G>C	NCBI36
NG_032783.1:g.32799C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.1266C>G MANE Select	ENSP00000406012.2:p.Val422=
ENST00000397417.6:c.439C>G	ENSP00000380562.2:p.Leu147Val
ENST00000426508.6:c.1266C>G	ENSP00000406012.2:p.Val422=
ENST00000439987.6:n.1327C>G
NM_014714.3:c.1266C>G	NP_055529.2:p.Val422=
XM_005255725.3:c.1266C>G	XP_005255782.1:p.Val422=
XM_005255726.2:c.1266C>G	XP_005255783.1:p.Val422=
XM_006720989.2:c.1266C>G	XP_006721052.1:p.Val422=
XM_006720990.2:c.1266C>G	XP_006721053.1:p.Val422=
XM_006720991.2:c.1266C>G	XP_006721054.1:p.Val422=
XM_011522766.1:c.1266C>G	XP_011521068.1:p.Val422=
XM_011522767.1:c.291C>G	XP_011521069.1:p.Val97=
XM_011522768.1:c.1266C>G	XP_011521070.1:p.Val422=
XM_011522769.1:c.1266C>G	XP_011521071.1:p.Val422=
XM_011522771.1:c.1266C>G	XP_011521073.1:p.Val422=
XM_011522772.1:c.1266C>G	XP_011521074.1:p.Val422=
NR_135176.1:n.59+3725G>C
XM_005255725.5:c.1266C>G	XP_005255782.1:p.Val422=
XM_005255726.4:c.1266C>G	XP_005255783.1:p.Val422=
XM_006720990.3:c.1266C>G	XP_006721053.1:p.Val422=
XM_006720991.3:c.1266C>G	XP_006721054.1:p.Val422=
XM_011522766.3:c.1266C>G	XP_011521068.1:p.Val422=
XM_011522767.2:c.291C>G	XP_011521069.1:p.Val97=
XM_011522769.3:c.1266C>G	XP_011521071.1:p.Val422=
XM_011522771.3:c.1266C>G	XP_011521073.1:p.Val422=
XM_011522772.3:c.1266C>G	XP_011521074.1:p.Val422=
XM_017023910.1:c.1266C>G	XP_016879399.1:p.Val422=
XM_017023911.1:c.-432C>G	XP_016879400.1:n.-432C>G
NM_014714.4:c.1266C>G MANE Select	NP_055529.2:p.Val422=