Canonical Allele Identifier: CA391724490

Gene: IVD

Linked Data

• MyVariant Identifiers: chr15:g.40710379G>T (hg19) ; chr15:g.40418180G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40418180G>T , CM000677.2:g.40418180G>T	GRCh38
NC_000015.9:g.40710379G>T , CM000677.1:g.40710379G>T	GRCh37
NC_000015.8:g.38497671G>T	NCBI36
NG_011986.1:g.17694G>T
NG_011986.2:g.17696G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000479013.7:c.1099G>T	ENSP00000417990.3:p.Ala367Ser
ENST00000487418.8:c.1189G>T MANE Select	ENSP00000418397.3:p.Ala397Ser
ENST00000650656.1:c.1108G>T	ENSP00000498731.1:p.Ala370Ser
ENST00000651168.1:c.1198G>T	ENSP00000499074.1:p.Ala400Ser
ENST00000466756.2:c.89+1818G>T
ENST00000473112.6:c.719+2698G>T
ENST00000479013.6:c.1108G>T	ENSP00000417990.2:p.Ala370Ser
ENST00000481262.6:c.650+1818G>T
ENST00000487418.6:c.1198G>T	ENSP00000418397.2:p.Ala400Ser
ENST00000491554.6:c.535+1818G>T	ENSP00000453146.1:n.535+1818G>T
ENST00000497816.1:n.566G>T
ENST00000559575.5:c.102-1000G>T
NM_001159508.1:c.1108G>T	NP_001152980.1:p.Ala370Ser
NM_002225.3:c.1198G>T	NP_002216.2:p.Ala400Ser
XM_005254350.2:c.1147+1818G>T	XP_005254407.1:n.1147+1818G>T
XM_005254356.2:c.875+2698G>T	XP_005254413.1:n.875+2698G>T
XM_006720491.2:c.1090+1818G>T	XP_006720554.1:n.1090+1818G>T
XM_006720492.2:c.1147+1818G>T	XP_006720555.1:n.1147+1818G>T
XM_006720493.2:c.1147+1818G>T	XP_006720556.1:n.1147+1818G>T
XM_006720494.2:c.1148-1000G>T	XP_006720557.1:n.1148-1000G>T
XM_006720495.2:c.969+2698G>T	XP_006720558.1:n.969+2698G>T
XM_011521523.1:c.1147+1818G>T	XP_011519825.1:n.1147+1818G>T
XR_243097.3:n.1104G>T
XR_243098.2:n.1053+1818G>T
XR_429453.2:n.1299G>T
NM_001159508.2:c.1099G>T	NP_001152980.2:p.Ala367Ser
NM_001354597.2:c.1141G>T	NP_001341526.1:p.Ala381Ser
NM_001354598.2:c.1138+1818G>T	NP_001341527.2:n.1138+1818G>T
NM_001354599.2:c.1276G>T	NP_001341528.2:p.Ala426Ser
NM_001354600.2:c.1225+1818G>T	NP_001341529.2:n.1225+1818G>T
NM_001354601.2:c.1138+1818G>T	NP_001341530.2:n.1138+1818G>T
NM_002225.4:c.1189G>T	NP_002216.3:p.Ala397Ser
NR_148925.1:n.1548+1818G>T
XM_006720495.3:c.969+2698G>T	XP_006720558.1:n.969+2698G>T
XM_017022149.1:c.1234+1818G>T	XP_016877638.1:n.1234+1818G>T
XM_017022150.1:c.1234+1818G>T	XP_016877639.1:n.1234+1818G>T
XM_017022153.1:c.1234+1818G>T	XP_016877642.1:n.1234+1818G>T
XM_017022154.2:c.1228G>T	XP_016877643.1:p.Ala410Ser
XM_017022155.2:c.1235-1000G>T	XP_016877644.1:n.1235-1000G>T
XM_017022157.1:c.1056+2698G>T	XP_016877646.1:n.1056+2698G>T
XR_001751263.1:n.1548G>T
NM_001159508.3:c.1099G>T	NP_001152980.2:p.Ala367Ser
NM_001354597.3:c.1141G>T	NP_001341526.1:p.Ala381Ser
NM_001354598.3:c.1138+1818G>T	NP_001341527.2:n.1138+1818G>T
NM_001354599.3:c.1276G>T	NP_001341528.2:p.Ala426Ser
NM_001354600.3:c.1225+1818G>T	NP_001341529.2:n.1225+1818G>T
NM_001354601.3:c.1138+1818G>T	NP_001341530.2:n.1138+1818G>T
NM_002225.5:c.1189G>T MANE Select	NP_002216.3:p.Ala397Ser
NR_148925.2:n.1550+1818G>T