Canonical Allele Identifier: CA373266623

Gene: DNAI1

Linked Data

• MyVariant Identifiers: chr9:g.34517349A>T (hg19) ; chr9:g.34517351A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517351A>T , CM000671.2:g.34517351A>T	GRCh38
NC_000009.11:g.34517349A>T , CM000671.1:g.34517349A>T	GRCh37
NC_000009.10:g.34507349A>T	NCBI36
NG_008127.1:g.63539A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1885A>T MANE Select	ENSP00000242317.4:p.Lys629Ter
ENST00000242317.8:c.1885A>T	ENSP00000242317.4:p.Lys629Ter
ENST00000442556.1:c.329+2612A>T
ENST00000470169.5:c.673A>T
ENST00000485580.1:n.461A>T
ENST00000614641.4:c.1897A>T	ENSP00000480538.1:p.Lys633Ter
NM_001281428.1:c.1897A>T	NP_001268357.1:p.Lys633Ter
NM_012144.3:c.1885A>T	NP_036276.1:p.Lys629Ter
XM_006716758.2:c.1354A>T	XP_006716821.1:p.Lys452Ter
XM_011517848.1:c.1639A>T	XP_011516150.1:p.Lys547Ter
XM_006716758.3:c.1354A>T	XP_006716821.1:p.Lys452Ter
XM_011517848.2:c.1639A>T	XP_011516150.1:p.Lys547Ter
XM_017014625.2:c.1627A>T	XP_016870114.1:p.Lys543Ter
XR_002956774.1:n.1988A>T
NM_012144.4:c.1885A>T MANE Select	NP_036276.1:p.Lys629Ter
NM_001281428.2:c.1897A>T	NP_001268357.1:p.Lys633Ter