Canonical Allele Identifier: CA373246784

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34490411C>T , CM000671.2:g.34490411C>T	GRCh38
NC_000009.11:g.34490409C>T , CM000671.1:g.34490409C>T	GRCh37
NC_000009.10:g.34480409C>T	NCBI36
NG_008127.1:g.36599C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_012144.4:c.544C>T MANE Select	NP_036276.1:p.Gln182Ter
ENST00000242317.9:c.544C>T MANE Select	ENSP00000242317.4:p.Gln182Ter
NM_001281428.1:c.556C>T	NP_001268357.1:p.Gln186Ter
NM_001281428.2:c.556C>T	NP_001268357.1:p.Gln186Ter
NM_012144.3:c.544C>T	NP_036276.1:p.Gln182Ter
ENST00000242317.8:c.544C>T	ENSP00000242317.4:p.Gln182Ter
ENST00000437363.5:c.511C>T	ENSP00000395396.1:p.Gln171Ter
ENST00000488369.1:n.660C>T
ENST00000614641.4:c.556C>T	ENSP00000480538.1:p.Gln186Ter
XM_006716758.2:c.13C>T	XP_006716821.1:p.Gln5Ter
XM_006716758.3:c.13C>T	XP_006716821.1:p.Gln5Ter
XM_011517846.1:c.556C>T	XP_011516148.1:p.Gln186Ter
XM_011517846.2:c.556C>T	XP_011516148.1:p.Gln186Ter
XM_011517847.1:c.556C>T	XP_011516149.1:p.Gln186Ter
XM_011517847.3:c.556C>T	XP_011516149.1:p.Gln186Ter
XM_011517848.1:c.556C>T	XP_011516150.1:p.Gln186Ter
XM_011517848.2:c.556C>T	XP_011516150.1:p.Gln186Ter
XM_011517849.1:c.556C>T	XP_011516151.1:p.Gln186Ter
XM_011517849.2:c.556C>T	XP_011516151.1:p.Gln186Ter
XM_011517850.1:c.556C>T	XP_011516152.1:p.Gln186Ter
XM_011517850.3:c.556C>T	XP_011516152.1:p.Gln186Ter
XM_017014625.2:c.544C>T	XP_016870114.1:p.Gln182Ter
XR_002956774.1:n.757C>T
XR_929232.1:n.810C>T
XR_929232.2:n.757C>T
XR_929233.1:n.810C>T
XR_929233.2:n.757C>T
XR_929235.1:n.810C>T