Canonical Allele Identifier: CA2171765928

Gene: IVD

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40411543_40411544delinsTC , CM000677.2:g.40411543_40411544delinsTC	GRCh38
NC_000015.9:g.40703742_40703743delinsTC , CM000677.1:g.40703742_40703743delinsTC	GRCh37
NC_000015.8:g.38491034_38491035delinsTC	NCBI36
NG_011986.1:g.11057_11058delinsTC
NG_011986.2:g.11059_11060delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.461-12_461-11delinsTC	ENSP00000417990.3:n.461-12_461-11delinsTC
ENST00000487418.8:c.551-12_551-11delinsTC MANE Select	ENSP00000418397.3:n.551-12_551-11delinsTC
ENST00000650656.1:c.470-12_470-11delinsTC	ENSP00000498731.1:n.470-12_470-11delinsTC
ENST00000651168.1:c.560-12_560-11delinsTC	ENSP00000499074.1:n.560-12_560-11delinsTC
ENST00000473112.6:c.310-12_310-11delinsTC
ENST00000479013.6:c.470-12_470-11delinsTC	ENSP00000417990.2:n.470-12_470-11delinsTC
ENST00000481262.6:c.157-12_157-11delinsTC
ENST00000484250.1:n.174-12_174-11delinsTC
ENST00000487418.6:c.560-12_560-11delinsTC	ENSP00000418397.2:n.560-12_560-11delinsTC
ENST00000558610.5:c.503-12_503-11delinsTC	ENSP00000453821.1:n.503-12_503-11delinsTC
NM_001159508.1:c.470-12_470-11delinsTC	NP_001152980.1:n.470-12_470-11delinsTC
NM_002225.3:c.560-12_560-11delinsTC	NP_002216.2:n.560-12_560-11delinsTC
XM_005254350.2:c.560-12_560-11delinsTC	XP_005254407.1:n.560-12_560-11delinsTC
XM_005254356.2:c.560-12_560-11delinsTC	XP_005254413.1:n.560-12_560-11delinsTC
XM_006720491.2:c.503-12_503-11delinsTC	XP_006720554.1:n.503-12_503-11delinsTC
XM_006720492.2:c.560-12_560-11delinsTC	XP_006720555.1:n.560-12_560-11delinsTC
XM_006720493.2:c.560-12_560-11delinsTC	XP_006720556.1:n.560-12_560-11delinsTC
XM_006720494.2:c.560-12_560-11delinsTC	XP_006720557.1:n.560-12_560-11delinsTC
XM_006720495.2:c.560-12_560-11delinsTC	XP_006720558.1:n.560-12_560-11delinsTC
XM_011521523.1:c.560-12_560-11delinsTC	XP_011519825.1:n.560-12_560-11delinsTC
XM_011521524.1:c.560-12_560-11delinsTC	XP_011519826.1:n.560-12_560-11delinsTC
XR_243097.3:n.560-12_560-11delinsTC
XR_243098.2:n.560-12_560-11delinsTC
XR_429453.2:n.661-12_661-11delinsTC
NM_001159508.2:c.461-12_461-11delinsTC	NP_001152980.2:n.461-12_461-11delinsTC
NM_001354597.2:c.503-12_503-11delinsTC	NP_001341526.1:n.503-12_503-11delinsTC
NM_001354598.2:c.551-12_551-11delinsTC	NP_001341527.2:n.551-12_551-11delinsTC
NM_001354599.2:c.638-12_638-11delinsTC	NP_001341528.2:n.638-12_638-11delinsTC
NM_001354600.2:c.638-12_638-11delinsTC	NP_001341529.2:n.638-12_638-11delinsTC
NM_001354601.2:c.551-12_551-11delinsTC	NP_001341530.2:n.551-12_551-11delinsTC
NM_002225.4:c.551-12_551-11delinsTC	NP_002216.3:n.551-12_551-11delinsTC
NR_148925.1:n.961-12_961-11delinsTC
XM_006720495.3:c.560-12_560-11delinsTC	XP_006720558.1:n.560-12_560-11delinsTC
XM_017022149.1:c.647-12_647-11delinsTC	XP_016877638.1:n.647-12_647-11delinsTC
XM_017022150.1:c.647-12_647-11delinsTC	XP_016877639.1:n.647-12_647-11delinsTC
XM_017022153.1:c.647-12_647-11delinsTC	XP_016877642.1:n.647-12_647-11delinsTC
XM_017022154.2:c.590-12_590-11delinsTC	XP_016877643.1:n.590-12_590-11delinsTC
XM_017022155.2:c.647-12_647-11delinsTC	XP_016877644.1:n.647-12_647-11delinsTC
XM_017022157.1:c.647-12_647-11delinsTC	XP_016877646.1:n.647-12_647-11delinsTC
XM_017022158.2:c.647-12_647-11delinsTC	XP_016877647.1:n.647-12_647-11delinsTC
XR_001751263.1:n.910-12_910-11delinsTC
XR_001751264.1:n.951-12_951-11delinsTC
NM_001159508.3:c.461-12_461-11delinsTC	NP_001152980.2:n.461-12_461-11delinsTC
NM_001354597.3:c.503-12_503-11delinsTC	NP_001341526.1:n.503-12_503-11delinsTC
NM_001354598.3:c.551-12_551-11delinsTC	NP_001341527.2:n.551-12_551-11delinsTC
NM_001354599.3:c.638-12_638-11delinsTC	NP_001341528.2:n.638-12_638-11delinsTC
NM_001354600.3:c.638-12_638-11delinsTC	NP_001341529.2:n.638-12_638-11delinsTC
NM_001354601.3:c.551-12_551-11delinsTC	NP_001341530.2:n.551-12_551-11delinsTC
NM_002225.5:c.551-12_551-11delinsTC MANE Select	NP_002216.3:n.551-12_551-11delinsTC
NR_148925.2:n.963-12_963-11delinsTC