Canonical Allele Identifier: CA391746080

Gene: IVD

Linked Data

• MyVariant Identifiers: chr15:g.40700186C>G (hg19) ; chr15:g.40407987C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40407987C>G , CM000677.2:g.40407987C>G	GRCh38
NC_000015.9:g.40700186C>G , CM000677.1:g.40700186C>G	GRCh37
NC_000015.8:g.38487478C>G	NCBI36
NG_011986.1:g.7501C>G
NG_011986.2:g.7503C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.193C>G	ENSP00000417990.3:p.Pro65Ala
ENST00000487418.8:c.283C>G MANE Select	ENSP00000418397.3:p.Pro95Ala
ENST00000610693.5:c.370C>G	ENSP00000479359.2:p.Pro124Ala
ENST00000650656.1:c.202C>G	ENSP00000498731.1:p.Pro68Ala
ENST00000651168.1:c.292C>G	ENSP00000499074.1:p.Pro98Ala
ENST00000473112.6:c.42C>G
ENST00000479013.6:c.202C>G	ENSP00000417990.2:p.Pro68Ala
ENST00000487418.6:c.292C>G	ENSP00000418397.2:p.Pro98Ala
ENST00000558610.5:c.235C>G	ENSP00000453821.1:p.Pro79Ala
ENST00000610693.4:c.379C>G	ENSP00000479359.1:p.Pro127Ala
NM_001159508.1:c.202C>G	NP_001152980.1:p.Pro68Ala
NM_002225.3:c.292C>G	NP_002216.2:p.Pro98Ala
XM_005254350.2:c.292C>G	XP_005254407.1:p.Pro98Ala
XM_005254356.2:c.292C>G	XP_005254413.1:p.Pro98Ala
XM_006720491.2:c.235C>G	XP_006720554.1:p.Pro79Ala
XM_006720492.2:c.292C>G	XP_006720555.1:p.Pro98Ala
XM_006720493.2:c.292C>G	XP_006720556.1:p.Pro98Ala
XM_006720494.2:c.292C>G	XP_006720557.1:p.Pro98Ala
XM_006720495.2:c.292C>G	XP_006720558.1:p.Pro98Ala
XM_011521523.1:c.292C>G	XP_011519825.1:p.Pro98Ala
XM_011521524.1:c.292C>G	XP_011519826.1:p.Pro98Ala
XR_243097.3:n.292C>G
XR_243098.2:n.292C>G
XR_429453.2:n.393C>G
NM_001159508.2:c.193C>G	NP_001152980.2:p.Pro65Ala
NM_001354597.2:c.235C>G	NP_001341526.1:p.Pro79Ala
NM_001354598.2:c.283C>G	NP_001341527.2:p.Pro95Ala
NM_001354599.2:c.370C>G	NP_001341528.2:p.Pro124Ala
NM_001354600.2:c.370C>G	NP_001341529.2:p.Pro124Ala
NM_001354601.2:c.283C>G	NP_001341530.2:p.Pro95Ala
NM_002225.4:c.283C>G	NP_002216.3:p.Pro95Ala
NR_148925.1:n.693C>G
XM_006720495.3:c.292C>G	XP_006720558.1:p.Pro98Ala
XM_017022149.1:c.379C>G	XP_016877638.1:p.Pro127Ala
XM_017022150.1:c.379C>G	XP_016877639.1:p.Pro127Ala
XM_017022153.1:c.379C>G	XP_016877642.1:p.Pro127Ala
XM_017022154.2:c.322C>G	XP_016877643.1:p.Pro108Ala
XM_017022155.2:c.379C>G	XP_016877644.1:p.Pro127Ala
XM_017022157.1:c.379C>G	XP_016877646.1:p.Pro127Ala
XM_017022158.2:c.379C>G	XP_016877647.1:p.Pro127Ala
XR_001751263.1:n.642C>G
XR_001751264.1:n.683C>G
NM_001159508.3:c.193C>G	NP_001152980.2:p.Pro65Ala
NM_001354597.3:c.235C>G	NP_001341526.1:p.Pro79Ala
NM_001354598.3:c.283C>G	NP_001341527.2:p.Pro95Ala
NM_001354599.3:c.370C>G	NP_001341528.2:p.Pro124Ala
NM_001354600.3:c.370C>G	NP_001341529.2:p.Pro124Ala
NM_001354601.3:c.283C>G	NP_001341530.2:p.Pro95Ala
NM_002225.5:c.283C>G MANE Select	NP_002216.3:p.Pro95Ala
NR_148925.2:n.695C>G