Canonical Allele Identifier: CA2627813720

Gene: IVD

Linked Data

• gnomAD v4: 15-40411150-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40411154_40411155del , CM000677.2:g.40411154_40411155del	GRCh38
NC_000015.9:g.40703353_40703354del , CM000677.1:g.40703353_40703354del	GRCh37
NC_000015.8:g.38490645_38490646del	NCBI36
NG_011986.1:g.10668_10669del
NG_011986.2:g.10670_10671del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.367-106_367-105del	ENSP00000417990.3:n.367-106_367-105del
ENST00000487418.8:c.457-106_457-105del MANE Select	ENSP00000418397.3:n.457-106_457-105del
ENST00000610693.5:c.544-106_544-105del	ENSP00000479359.2:n.544-106_544-105del
ENST00000650656.1:c.376-106_376-105del	ENSP00000498731.1:n.376-106_376-105del
ENST00000651168.1:c.466-106_466-105del	ENSP00000499074.1:n.466-106_466-105del
ENST00000473112.6:c.216-106_216-105del
ENST00000479013.6:c.376-106_376-105del	ENSP00000417990.2:n.376-106_376-105del
ENST00000481262.6:c.63-106_63-105del
ENST00000484250.1:n.80-106_80-105del
ENST00000487418.6:c.466-106_466-105del	ENSP00000418397.2:n.466-106_466-105del
ENST00000558610.5:c.409-106_409-105del	ENSP00000453821.1:n.409-106_409-105del
ENST00000610693.4:c.553-106_553-105del	ENSP00000479359.1:n.553-106_553-105del
NM_001159508.1:c.376-106_376-105del	NP_001152980.1:n.376-106_376-105del
NM_002225.3:c.466-106_466-105del	NP_002216.2:n.466-106_466-105del
XM_005254350.2:c.466-106_466-105del	XP_005254407.1:n.466-106_466-105del
XM_005254356.2:c.466-106_466-105del	XP_005254413.1:n.466-106_466-105del
XM_006720491.2:c.409-106_409-105del	XP_006720554.1:n.409-106_409-105del
XM_006720492.2:c.466-106_466-105del	XP_006720555.1:n.466-106_466-105del
XM_006720493.2:c.466-106_466-105del	XP_006720556.1:n.466-106_466-105del
XM_006720494.2:c.466-106_466-105del	XP_006720557.1:n.466-106_466-105del
XM_006720495.2:c.466-106_466-105del	XP_006720558.1:n.466-106_466-105del
XM_011521523.1:c.466-106_466-105del	XP_011519825.1:n.466-106_466-105del
XM_011521524.1:c.466-106_466-105del	XP_011519826.1:n.466-106_466-105del
XR_243097.3:n.466-106_466-105del
XR_243098.2:n.466-106_466-105del
XR_429453.2:n.567-106_567-105del
NM_001159508.2:c.367-106_367-105del	NP_001152980.2:n.367-106_367-105del
NM_001354597.2:c.409-106_409-105del	NP_001341526.1:n.409-106_409-105del
NM_001354598.2:c.457-106_457-105del	NP_001341527.2:n.457-106_457-105del
NM_001354599.2:c.544-106_544-105del	NP_001341528.2:n.544-106_544-105del
NM_001354600.2:c.544-106_544-105del	NP_001341529.2:n.544-106_544-105del
NM_001354601.2:c.457-106_457-105del	NP_001341530.2:n.457-106_457-105del
NM_002225.4:c.457-106_457-105del	NP_002216.3:n.457-106_457-105del
NR_148925.1:n.867-106_867-105del
XM_006720495.3:c.466-106_466-105del	XP_006720558.1:n.466-106_466-105del
XM_017022149.1:c.553-106_553-105del	XP_016877638.1:n.553-106_553-105del
XM_017022150.1:c.553-106_553-105del	XP_016877639.1:n.553-106_553-105del
XM_017022153.1:c.553-106_553-105del	XP_016877642.1:n.553-106_553-105del
XM_017022154.2:c.496-106_496-105del	XP_016877643.1:n.496-106_496-105del
XM_017022155.2:c.553-106_553-105del	XP_016877644.1:n.553-106_553-105del
XM_017022157.1:c.553-106_553-105del	XP_016877646.1:n.553-106_553-105del
XM_017022158.2:c.553-106_553-105del	XP_016877647.1:n.553-106_553-105del
XR_001751263.1:n.816-106_816-105del
XR_001751264.1:n.857-106_857-105del
NM_001159508.3:c.367-106_367-105del	NP_001152980.2:n.367-106_367-105del
NM_001354597.3:c.409-106_409-105del	NP_001341526.1:n.409-106_409-105del
NM_001354598.3:c.457-106_457-105del	NP_001341527.2:n.457-106_457-105del
NM_001354599.3:c.544-106_544-105del	NP_001341528.2:n.544-106_544-105del
NM_001354600.3:c.544-106_544-105del	NP_001341529.2:n.544-106_544-105del
NM_001354601.3:c.457-106_457-105del	NP_001341530.2:n.457-106_457-105del
NM_002225.5:c.457-106_457-105del MANE Select	NP_002216.3:n.457-106_457-105del
NR_148925.2:n.869-106_869-105del