Canonical Allele Identifier: CA7812845

Gene: IFT140

Linked Data

• dbSNP Id: rs778381028
• ExAC: 16:1561189 ACAACCAGGCACGACCC / A
• gnomAD v2: 16-1561189-ACAACCAGGCACGACCC-A
• gnomAD v4: 16-1511188-ACAACCAGGCACGACCC-A
• MyVariant Identifiers: chr16:g.1561190_1561205del (hg19) ; chr16:g.1511189_1511204del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511189_1511204del , CM000678.2:g.1511189_1511204del	GRCh38
NC_000016.9:g.1561190_1561205del , CM000678.1:g.1561190_1561205del	GRCh37
NC_000016.8:g.1501191_1501206del	NCBI36
NG_032783.1:g.105905_105920del
NG_050910.1:g.22846_22861del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4183-54_4183-39del MANE Select	ENSP00000406012.2:n.4183-54_4183-39del
ENST00000361339.9:c.1765-54_1765-39del	ENSP00000354895.5:n.1765-54_1765-39del
ENST00000397417.6:c.*2621-54_*2621-39del	ENSP00000380562.2:n.*2621-54_*2621-39del
ENST00000426508.6:c.4183-54_4183-39del	ENSP00000406012.2:n.4183-54_4183-39del
ENST00000565298.5:n.4007-54_4007-39del
NM_014714.3:c.4183-54_4183-39del	NP_055529.2:n.4183-54_4183-39del
XM_006720989.2:c.4183-54_4183-39del	XP_006721052.1:n.4183-54_4183-39del
XM_006720990.2:c.4183-54_4183-39del	XP_006721053.1:n.4183-54_4183-39del
XM_006720991.2:c.4183-54_4183-39del	XP_006721054.1:n.4183-54_4183-39del
XM_006720992.2:c.1816-54_1816-39del	XP_006721055.1:n.1816-54_1816-39del
XM_011522766.1:c.3937-54_3937-39del	XP_011521068.1:n.3937-54_3937-39del
XM_011522767.1:c.3208-54_3208-39del	XP_011521069.1:n.3208-54_3208-39del
XM_006720990.3:c.4183-54_4183-39del	XP_006721053.1:n.4183-54_4183-39del
XM_006720991.3:c.4183-54_4183-39del	XP_006721054.1:n.4183-54_4183-39del
XM_006720992.3:c.1816-54_1816-39del	XP_006721055.1:n.1816-54_1816-39del
XM_011522766.3:c.3937-54_3937-39del	XP_011521068.1:n.3937-54_3937-39del
XM_011522767.2:c.3208-54_3208-39del	XP_011521069.1:n.3208-54_3208-39del
XM_017023910.1:c.4183-54_4183-39del	XP_016879399.1:n.4183-54_4183-39del
XM_017023911.1:c.2368-54_2368-39del	XP_016879400.1:n.2368-54_2368-39del
NM_014714.4:c.4183-54_4183-39del MANE Select	NP_055529.2:n.4183-54_4183-39del