Canonical Allele Identifier: CA2575679061

Gene: IVD

Linked Data

• gnomAD v4: 15-40407749-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40407754del , CM000677.2:g.40407754del	GRCh38
NC_000015.9:g.40699955del , CM000677.1:g.40699955del	GRCh37
NC_000015.8:g.38487247del	NCBI36
NG_011986.1:g.7270del
NG_011986.2:g.7270del

Transcript Alleles

HGVS	Amino-acid change
ENST00000479013.7:c.145-185del	ENSP00000417990.3:n.145-185del
ENST00000487418.8:c.234+29del MANE Select	ENSP00000418397.3:n.234+29del
ENST00000610693.5:c.263del	ENSP00000479359.2:p.Gly88AlafsTer7
ENST00000650656.1:c.154-185del	ENSP00000498731.1:n.154-185del
ENST00000651168.1:c.243+29del	ENSP00000499074.1:n.243+29del
ENST00000479013.6:c.154-185del	ENSP00000417990.2:n.154-185del
ENST00000487418.6:c.243+29del	ENSP00000418397.2:n.243+29del
ENST00000558610.5:c.186+29del	ENSP00000453821.1:n.186+29del
ENST00000610693.4:c.272del	ENSP00000479359.1:p.Gly91AlafsTer7
NM_001159508.1:c.154-185del	NP_001152980.1:n.154-185del
NM_002225.3:c.243+29del	NP_002216.2:n.243+29del
XM_005254350.2:c.243+29del	XP_005254407.1:n.243+29del
XM_005254356.2:c.243+29del	XP_005254413.1:n.243+29del
XM_006720491.2:c.186+29del	XP_006720554.1:n.186+29del
XM_006720492.2:c.243+29del	XP_006720555.1:n.243+29del
XM_006720493.2:c.243+29del	XP_006720556.1:n.243+29del
XM_006720494.2:c.243+29del	XP_006720557.1:n.243+29del
XM_006720495.2:c.243+29del	XP_006720558.1:n.243+29del
XM_011521523.1:c.243+29del	XP_011519825.1:n.243+29del
XM_011521524.1:c.243+29del	XP_011519826.1:n.243+29del
XR_243097.3:n.243+29del
XR_243098.2:n.243+29del
XR_429453.2:n.344+29del
NM_001159508.2:c.145-185del	NP_001152980.2:n.145-185del
NM_001354597.2:c.186+29del	NP_001341526.1:n.186+29del
NM_001354598.2:c.234+29del	NP_001341527.2:n.234+29del
NM_001354599.2:c.263del	NP_001341528.2:p.Gly88AlafsTer7
NM_001354600.2:c.263del	NP_001341529.2:p.Gly88AlafsTer7
NM_001354601.2:c.234+29del	NP_001341530.2:n.234+29del
NM_002225.4:c.234+29del	NP_002216.3:n.234+29del
NR_148925.1:n.644+29del
XM_006720495.3:c.243+29del	XP_006720558.1:n.243+29del
XM_017022149.1:c.272del	XP_016877638.1:p.Gly91AlafsTer7
XM_017022150.1:c.272del	XP_016877639.1:p.Gly91AlafsTer7
XM_017022153.1:c.272del	XP_016877642.1:p.Gly91AlafsTer7
XM_017022154.2:c.215del	XP_016877643.1:p.Gly72AlafsTer7
XM_017022155.2:c.272del	XP_016877644.1:p.Gly91AlafsTer7
XM_017022157.1:c.272del	XP_016877646.1:p.Gly91AlafsTer7
XM_017022158.2:c.272del	XP_016877647.1:p.Gly91AlafsTer7
XR_001751263.1:n.593+29del
XR_001751264.1:n.634+29del
NM_001159508.3:c.145-185del	NP_001152980.2:n.145-185del
NM_001354597.3:c.186+29del	NP_001341526.1:n.186+29del
NM_001354598.3:c.234+29del	NP_001341527.2:n.234+29del
NM_001354599.3:c.263del	NP_001341528.2:p.Gly88AlafsTer7
NM_001354600.3:c.263del	NP_001341529.2:p.Gly88AlafsTer7
NM_001354601.3:c.234+29del	NP_001341530.2:n.234+29del
NM_002225.5:c.234+29del MANE Select	NP_002216.3:n.234+29del
NR_148925.2:n.646+29del