Canonical Allele Identifier: CA391717542

Gene: IVD

Linked Data

• MyVariant Identifiers: chr15:g.40703784T>G (hg19) ; chr15:g.40411585T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40411585T>G , CM000677.2:g.40411585T>G	GRCh38
NC_000015.9:g.40703784T>G , CM000677.1:g.40703784T>G	GRCh37
NC_000015.8:g.38491076T>G	NCBI36
NG_011986.1:g.11099T>G
NG_011986.2:g.11101T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.491T>G	ENSP00000417990.3:p.Phe164Cys
ENST00000487418.8:c.581T>G MANE Select	ENSP00000418397.3:p.Phe194Cys
ENST00000650656.1:c.500T>G	ENSP00000498731.1:p.Phe167Cys
ENST00000651168.1:c.590T>G	ENSP00000499074.1:p.Phe197Cys
ENST00000473112.6:c.340T>G
ENST00000479013.6:c.500T>G	ENSP00000417990.2:p.Phe167Cys
ENST00000481262.6:c.187T>G
ENST00000484250.1:n.204T>G
ENST00000487418.6:c.590T>G	ENSP00000418397.2:p.Phe197Cys
ENST00000558610.5:c.533T>G	ENSP00000453821.1:p.Phe178Cys
NM_001159508.1:c.500T>G	NP_001152980.1:p.Phe167Cys
NM_002225.3:c.590T>G	NP_002216.2:p.Phe197Cys
XM_005254350.2:c.590T>G	XP_005254407.1:p.Phe197Cys
XM_005254356.2:c.590T>G	XP_005254413.1:p.Phe197Cys
XM_006720491.2:c.533T>G	XP_006720554.1:p.Phe178Cys
XM_006720492.2:c.590T>G	XP_006720555.1:p.Phe197Cys
XM_006720493.2:c.590T>G	XP_006720556.1:p.Phe197Cys
XM_006720494.2:c.590T>G	XP_006720557.1:p.Phe197Cys
XM_006720495.2:c.590T>G	XP_006720558.1:p.Phe197Cys
XM_011521523.1:c.590T>G	XP_011519825.1:p.Phe197Cys
XM_011521524.1:c.590T>G	XP_011519826.1:p.Phe197Cys
XR_243097.3:n.590T>G
XR_243098.2:n.590T>G
XR_429453.2:n.691T>G
NM_001159508.2:c.491T>G	NP_001152980.2:p.Phe164Cys
NM_001354597.2:c.533T>G	NP_001341526.1:p.Phe178Cys
NM_001354598.2:c.581T>G	NP_001341527.2:p.Phe194Cys
NM_001354599.2:c.668T>G	NP_001341528.2:p.Phe223Cys
NM_001354600.2:c.668T>G	NP_001341529.2:p.Phe223Cys
NM_001354601.2:c.581T>G	NP_001341530.2:p.Phe194Cys
NM_002225.4:c.581T>G	NP_002216.3:p.Phe194Cys
NR_148925.1:n.991T>G
XM_006720495.3:c.590T>G	XP_006720558.1:p.Phe197Cys
XM_017022149.1:c.677T>G	XP_016877638.1:p.Phe226Cys
XM_017022150.1:c.677T>G	XP_016877639.1:p.Phe226Cys
XM_017022153.1:c.677T>G	XP_016877642.1:p.Phe226Cys
XM_017022154.2:c.620T>G	XP_016877643.1:p.Phe207Cys
XM_017022155.2:c.677T>G	XP_016877644.1:p.Phe226Cys
XM_017022157.1:c.677T>G	XP_016877646.1:p.Phe226Cys
XM_017022158.2:c.677T>G	XP_016877647.1:p.Phe226Cys
XR_001751263.1:n.940T>G
XR_001751264.1:n.981T>G
NM_001159508.3:c.491T>G	NP_001152980.2:p.Phe164Cys
NM_001354597.3:c.533T>G	NP_001341526.1:p.Phe178Cys
NM_001354598.3:c.581T>G	NP_001341527.2:p.Phe194Cys
NM_001354599.3:c.668T>G	NP_001341528.2:p.Phe223Cys
NM_001354600.3:c.668T>G	NP_001341529.2:p.Phe223Cys
NM_001354601.3:c.581T>G	NP_001341530.2:p.Phe194Cys
NM_002225.5:c.581T>G MANE Select	NP_002216.3:p.Phe194Cys
NR_148925.2:n.993T>G