Canonical Allele Identifier: CA391717081

Gene: IVD

Linked Data

• MyVariant Identifiers: chr15:g.40703493T>G (hg19) ; chr15:g.40411294T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40411294T>G , CM000677.2:g.40411294T>G	GRCh38
NC_000015.9:g.40703493T>G , CM000677.1:g.40703493T>G	GRCh37
NC_000015.8:g.38490785T>G	NCBI36
NG_011986.1:g.10808T>G
NG_011986.2:g.10810T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.401T>G	ENSP00000417990.3:p.Met134Arg
ENST00000487418.8:c.491T>G MANE Select	ENSP00000418397.3:p.Met164Arg
ENST00000610693.5:c.578T>G	ENSP00000479359.2:p.Met193Arg
ENST00000650656.1:c.410T>G	ENSP00000498731.1:p.Met137Arg
ENST00000651168.1:c.500T>G	ENSP00000499074.1:p.Met167Arg
ENST00000473112.6:c.250T>G
ENST00000479013.6:c.410T>G	ENSP00000417990.2:p.Met137Arg
ENST00000481262.6:c.97T>G
ENST00000484250.1:n.114T>G
ENST00000487418.6:c.500T>G	ENSP00000418397.2:p.Met167Arg
ENST00000558610.5:c.443T>G	ENSP00000453821.1:p.Met148Arg
ENST00000610693.4:c.587T>G	ENSP00000479359.1:p.Met196Arg
NM_001159508.1:c.410T>G	NP_001152980.1:p.Met137Arg
NM_002225.3:c.500T>G	NP_002216.2:p.Met167Arg
XM_005254350.2:c.500T>G	XP_005254407.1:p.Met167Arg
XM_005254356.2:c.500T>G	XP_005254413.1:p.Met167Arg
XM_006720491.2:c.443T>G	XP_006720554.1:p.Met148Arg
XM_006720492.2:c.500T>G	XP_006720555.1:p.Met167Arg
XM_006720493.2:c.500T>G	XP_006720556.1:p.Met167Arg
XM_006720494.2:c.500T>G	XP_006720557.1:p.Met167Arg
XM_006720495.2:c.500T>G	XP_006720558.1:p.Met167Arg
XM_011521523.1:c.500T>G	XP_011519825.1:p.Met167Arg
XM_011521524.1:c.500T>G	XP_011519826.1:p.Met167Arg
XR_243097.3:n.500T>G
XR_243098.2:n.500T>G
XR_429453.2:n.601T>G
NM_001159508.2:c.401T>G	NP_001152980.2:p.Met134Arg
NM_001354597.2:c.443T>G	NP_001341526.1:p.Met148Arg
NM_001354598.2:c.491T>G	NP_001341527.2:p.Met164Arg
NM_001354599.2:c.578T>G	NP_001341528.2:p.Met193Arg
NM_001354600.2:c.578T>G	NP_001341529.2:p.Met193Arg
NM_001354601.2:c.491T>G	NP_001341530.2:p.Met164Arg
NM_002225.4:c.491T>G	NP_002216.3:p.Met164Arg
NR_148925.1:n.901T>G
XM_006720495.3:c.500T>G	XP_006720558.1:p.Met167Arg
XM_017022149.1:c.587T>G	XP_016877638.1:p.Met196Arg
XM_017022150.1:c.587T>G	XP_016877639.1:p.Met196Arg
XM_017022153.1:c.587T>G	XP_016877642.1:p.Met196Arg
XM_017022154.2:c.530T>G	XP_016877643.1:p.Met177Arg
XM_017022155.2:c.587T>G	XP_016877644.1:p.Met196Arg
XM_017022157.1:c.587T>G	XP_016877646.1:p.Met196Arg
XM_017022158.2:c.587T>G	XP_016877647.1:p.Met196Arg
XR_001751263.1:n.850T>G
XR_001751264.1:n.891T>G
NM_001159508.3:c.401T>G	NP_001152980.2:p.Met134Arg
NM_001354597.3:c.443T>G	NP_001341526.1:p.Met148Arg
NM_001354598.3:c.491T>G	NP_001341527.2:p.Met164Arg
NM_001354599.3:c.578T>G	NP_001341528.2:p.Met193Arg
NM_001354600.3:c.578T>G	NP_001341529.2:p.Met193Arg
NM_001354601.3:c.491T>G	NP_001341530.2:p.Met164Arg
NM_002225.5:c.491T>G MANE Select	NP_002216.3:p.Met164Arg
NR_148925.2:n.903T>G