Canonical Allele Identifier: CA464398334

Gene: DNAI1

Linked Data

• gnomAD v4: 9-34517311-C-T
• MyVariant Identifiers: chr9:g.34517309C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517311C>T , CM000671.2:g.34517311C>T	GRCh38
NC_000009.11:g.34517309C>T , CM000671.1:g.34517309C>T	GRCh37
NC_000009.10:g.34507309C>T	NCBI36
NG_008127.1:g.63499C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1845C>T MANE Select	ENSP00000242317.4:p.Asn615=
ENST00000242317.8:c.1845C>T	ENSP00000242317.4:p.Asn615=
ENST00000442556.1:c.329+2572C>T
ENST00000470169.5:c.633C>T
ENST00000485580.1:n.421C>T
ENST00000614641.4:c.1857C>T	ENSP00000480538.1:p.Asn619=
NM_001281428.1:c.1857C>T	NP_001268357.1:p.Asn619=
NM_012144.3:c.1845C>T	NP_036276.1:p.Asn615=
XM_006716758.2:c.1314C>T	XP_006716821.1:p.Asn438=
XM_011517848.1:c.1599C>T	XP_011516150.1:p.Asn533=
XM_006716758.3:c.1314C>T	XP_006716821.1:p.Asn438=
XM_011517848.2:c.1599C>T	XP_011516150.1:p.Asn533=
XM_017014625.2:c.1587C>T	XP_016870114.1:p.Asn529=
XR_002956774.1:n.1948C>T
NM_012144.4:c.1845C>T MANE Select	NP_036276.1:p.Asn615=
NM_001281428.2:c.1857C>T	NP_001268357.1:p.Asn619=