Canonical Allele Identifier: CA464594264

Gene: DNAI1

Linked Data

• MyVariant Identifiers: chr9:g.34514463C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34514465C>A , CM000671.2:g.34514465C>A	GRCh38
NC_000009.11:g.34514463C>A , CM000671.1:g.34514463C>A	GRCh37
NC_000009.10:g.34504463C>A	NCBI36
NG_008127.1:g.60653C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1641C>A MANE Select	ENSP00000242317.4:p.Ser547=
ENST00000242317.8:c.1641C>A	ENSP00000242317.4:p.Ser547=
ENST00000442556.1:c.152C>A
ENST00000470169.5:c.507-175C>A
ENST00000485580.1:n.120C>A
ENST00000614641.4:c.1653C>A	ENSP00000480538.1:p.Ser551=
NM_001281428.1:c.1653C>A	NP_001268357.1:p.Ser551=
NM_012144.3:c.1641C>A	NP_036276.1:p.Ser547=
XM_006716758.2:c.1110C>A	XP_006716821.1:p.Ser370=
XM_011517846.1:c.1653C>A	XP_011516148.1:p.Ser551=
XM_011517847.1:c.1653C>A	XP_011516149.1:p.Ser551=
XM_011517848.1:c.1395C>A	XP_011516150.1:p.Ser465=
XM_011517849.1:c.1582-39C>A	XP_011516151.1:n.1582-39C>A
XR_929232.1:n.1836-39C>A
XR_929233.1:n.1836-39C>A
XR_929235.1:n.1578-39C>A
XM_006716758.3:c.1110C>A	XP_006716821.1:p.Ser370=
XM_011517846.2:c.1653C>A	XP_011516148.1:p.Ser551=
XM_011517847.3:c.1653C>A	XP_011516149.1:p.Ser551=
XM_011517848.2:c.1395C>A	XP_011516150.1:p.Ser465=
XM_011517849.2:c.1582-39C>A	XP_011516151.1:n.1582-39C>A
XM_017014625.2:c.1383C>A	XP_016870114.1:p.Ser461=
XR_002956774.1:n.1783-39C>A
XR_929232.2:n.1783-39C>A
XR_929233.2:n.1783-39C>A
NM_012144.4:c.1641C>A MANE Select	NP_036276.1:p.Ser547=
NM_001281428.2:c.1653C>A	NP_001268357.1:p.Ser551=