Canonical Allele Identifier: CA2627812329

Gene: IVD

Linked Data

• gnomAD v4: 15-40407557-TTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40407560_40407561del , CM000677.2:g.40407560_40407561del	GRCh38
NC_000015.9:g.40699761_40699762del , CM000677.1:g.40699761_40699762del	GRCh37
NC_000015.8:g.38487053_38487054del	NCBI36
NG_011986.1:g.7076_7077del
NG_011986.2:g.7076_7077del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.145-379_145-378del	ENSP00000417990.3:n.145-379_145-378del
ENST00000487418.8:c.145-76_145-75del MANE Select	ENSP00000418397.3:n.145-76_145-75del
ENST00000610693.5:c.145-76_145-75del	ENSP00000479359.2:n.145-76_145-75del
ENST00000650656.1:c.154-379_154-378del	ENSP00000498731.1:n.154-379_154-378del
ENST00000651168.1:c.154-76_154-75del	ENSP00000499074.1:n.154-76_154-75del
ENST00000479013.6:c.154-379_154-378del	ENSP00000417990.2:n.154-379_154-378del
ENST00000487418.6:c.154-76_154-75del	ENSP00000418397.2:n.154-76_154-75del
ENST00000558610.5:c.97-76_97-75del	ENSP00000453821.1:n.97-76_97-75del
ENST00000610693.4:c.154-76_154-75del	ENSP00000479359.1:n.154-76_154-75del
NM_001159508.1:c.154-379_154-378del	NP_001152980.1:n.154-379_154-378del
NM_002225.3:c.154-76_154-75del	NP_002216.2:n.154-76_154-75del
XM_005254350.2:c.154-76_154-75del	XP_005254407.1:n.154-76_154-75del
XM_005254356.2:c.154-76_154-75del	XP_005254413.1:n.154-76_154-75del
XM_006720491.2:c.97-76_97-75del	XP_006720554.1:n.97-76_97-75del
XM_006720492.2:c.154-76_154-75del	XP_006720555.1:n.154-76_154-75del
XM_006720493.2:c.154-76_154-75del	XP_006720556.1:n.154-76_154-75del
XM_006720494.2:c.154-76_154-75del	XP_006720557.1:n.154-76_154-75del
XM_006720495.2:c.154-76_154-75del	XP_006720558.1:n.154-76_154-75del
XM_011521523.1:c.154-76_154-75del	XP_011519825.1:n.154-76_154-75del
XM_011521524.1:c.154-76_154-75del	XP_011519826.1:n.154-76_154-75del
XR_243097.3:n.154-76_154-75del
XR_243098.2:n.154-76_154-75del
XR_429453.2:n.255-76_255-75del
NM_001159508.2:c.145-379_145-378del	NP_001152980.2:n.145-379_145-378del
NM_001354597.2:c.97-76_97-75del	NP_001341526.1:n.97-76_97-75del
NM_001354598.2:c.145-76_145-75del	NP_001341527.2:n.145-76_145-75del
NM_001354599.2:c.145-76_145-75del	NP_001341528.2:n.145-76_145-75del
NM_001354600.2:c.145-76_145-75del	NP_001341529.2:n.145-76_145-75del
NM_001354601.2:c.145-76_145-75del	NP_001341530.2:n.145-76_145-75del
NM_002225.4:c.145-76_145-75del	NP_002216.3:n.145-76_145-75del
NR_148925.1:n.555-76_555-75del
XM_006720495.3:c.154-76_154-75del	XP_006720558.1:n.154-76_154-75del
XM_017022149.1:c.154-76_154-75del	XP_016877638.1:n.154-76_154-75del
XM_017022150.1:c.154-76_154-75del	XP_016877639.1:n.154-76_154-75del
XM_017022153.1:c.154-76_154-75del	XP_016877642.1:n.154-76_154-75del
XM_017022154.2:c.97-76_97-75del	XP_016877643.1:n.97-76_97-75del
XM_017022155.2:c.154-76_154-75del	XP_016877644.1:n.154-76_154-75del
XM_017022157.1:c.154-76_154-75del	XP_016877646.1:n.154-76_154-75del
XM_017022158.2:c.154-76_154-75del	XP_016877647.1:n.154-76_154-75del
XR_001751263.1:n.504-76_504-75del
XR_001751264.1:n.545-76_545-75del
NM_001159508.3:c.145-379_145-378del	NP_001152980.2:n.145-379_145-378del
NM_001354597.3:c.97-76_97-75del	NP_001341526.1:n.97-76_97-75del
NM_001354598.3:c.145-76_145-75del	NP_001341527.2:n.145-76_145-75del
NM_001354599.3:c.145-76_145-75del	NP_001341528.2:n.145-76_145-75del
NM_001354600.3:c.145-76_145-75del	NP_001341529.2:n.145-76_145-75del
NM_001354601.3:c.145-76_145-75del	NP_001341530.2:n.145-76_145-75del
NM_002225.5:c.145-76_145-75del MANE Select	NP_002216.3:n.145-76_145-75del
NR_148925.2:n.557-76_557-75del