Canonical Allele Identifier: CA391717852

Gene: IVD

Linked Data

• MyVariant Identifiers: chr15:g.40703859C>T (hg19) ; chr15:g.40411660C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40411660C>T , CM000677.2:g.40411660C>T	GRCh38
NC_000015.9:g.40703859C>T , CM000677.1:g.40703859C>T	GRCh37
NC_000015.8:g.38491151C>T	NCBI36
NG_011986.1:g.11174C>T
NG_011986.2:g.11176C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.566C>T	ENSP00000417990.3:p.Ser189Phe
ENST00000487418.8:c.656C>T MANE Select	ENSP00000418397.3:p.Ser219Phe
ENST00000650656.1:c.575C>T	ENSP00000498731.1:p.Ser192Phe
ENST00000651168.1:c.665C>T	ENSP00000499074.1:p.Ser222Phe
ENST00000473112.6:c.415C>T
ENST00000479013.6:c.575C>T	ENSP00000417990.2:p.Ser192Phe
ENST00000481262.6:c.262C>T
ENST00000484250.1:n.279C>T
ENST00000487418.6:c.665C>T	ENSP00000418397.2:p.Ser222Phe
ENST00000491554.6:c.53C>T	ENSP00000453146.1:p.Ser18Phe
ENST00000558610.5:c.608C>T	ENSP00000453821.1:p.Ser203Phe
NM_001159508.1:c.575C>T	NP_001152980.1:p.Ser192Phe
NM_002225.3:c.665C>T	NP_002216.2:p.Ser222Phe
XM_005254350.2:c.665C>T	XP_005254407.1:p.Ser222Phe
XM_005254356.2:c.665C>T	XP_005254413.1:p.Ser222Phe
XM_006720491.2:c.608C>T	XP_006720554.1:p.Ser203Phe
XM_006720492.2:c.665C>T	XP_006720555.1:p.Ser222Phe
XM_006720493.2:c.665C>T	XP_006720556.1:p.Ser222Phe
XM_006720494.2:c.665C>T	XP_006720557.1:p.Ser222Phe
XM_006720495.2:c.665C>T	XP_006720558.1:p.Ser222Phe
XM_011521523.1:c.665C>T	XP_011519825.1:p.Ser222Phe
XM_011521524.1:c.665C>T	XP_011519826.1:p.Ser222Phe
XR_243097.3:n.665C>T
XR_243098.2:n.665C>T
XR_429453.2:n.766C>T
NM_001159508.2:c.566C>T	NP_001152980.2:p.Ser189Phe
NM_001354597.2:c.608C>T	NP_001341526.1:p.Ser203Phe
NM_001354598.2:c.656C>T	NP_001341527.2:p.Ser219Phe
NM_001354599.2:c.743C>T	NP_001341528.2:p.Ser248Phe
NM_001354600.2:c.743C>T	NP_001341529.2:p.Ser248Phe
NM_001354601.2:c.656C>T	NP_001341530.2:p.Ser219Phe
NM_002225.4:c.656C>T	NP_002216.3:p.Ser219Phe
NR_148925.1:n.1066C>T
XM_006720495.3:c.665C>T	XP_006720558.1:p.Ser222Phe
XM_017022149.1:c.752C>T	XP_016877638.1:p.Ser251Phe
XM_017022150.1:c.752C>T	XP_016877639.1:p.Ser251Phe
XM_017022153.1:c.752C>T	XP_016877642.1:p.Ser251Phe
XM_017022154.2:c.695C>T	XP_016877643.1:p.Ser232Phe
XM_017022155.2:c.752C>T	XP_016877644.1:p.Ser251Phe
XM_017022157.1:c.752C>T	XP_016877646.1:p.Ser251Phe
XM_017022158.2:c.752C>T	XP_016877647.1:p.Ser251Phe
XR_001751263.1:n.1015C>T
XR_001751264.1:n.1056C>T
NM_001159508.3:c.566C>T	NP_001152980.2:p.Ser189Phe
NM_001354597.3:c.608C>T	NP_001341526.1:p.Ser203Phe
NM_001354598.3:c.656C>T	NP_001341527.2:p.Ser219Phe
NM_001354599.3:c.743C>T	NP_001341528.2:p.Ser248Phe
NM_001354600.3:c.743C>T	NP_001341529.2:p.Ser248Phe
NM_001354601.3:c.656C>T	NP_001341530.2:p.Ser219Phe
NM_002225.5:c.656C>T MANE Select	NP_002216.3:p.Ser219Phe
NR_148925.2:n.1068C>T