Canonical Allele Identifier: CA1725903938
Gene: GATAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92448806T= , CM000669.2:g.92448806T= GRCh38
NC_000007.13:g.92078120T= , CM000669.1:g.92078120T= GRCh37
NC_000007.12:g.91916056T= NCBI36
NG_032807.1:g.6359T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287957.5:c.304T= MANE Select ENSP00000287957.3:p.Ser102=
ENST00000644160.1:n.160T=
ENST00000645746.1:c.304T= ENSP00000493785.1:p.Ser102=
ENST00000287957.3:c.304T= ENSP00000287957.3:p.Ser102=
NM_021167.4:c.304T= NP_066990.3:p.Ser102=
NR_052016.1:n.586T=
XR_428182.2:n.559T=
XR_927494.1:n.559T=
XR_927495.1:n.559T=
XR_927496.1:n.559T=
XR_927497.1:n.559T=
XR_927498.1:n.559T=
XR_927499.1:n.559T=
XR_927500.1:n.559T=
XR_927501.1:n.559T=
XR_927502.1:n.559T=
XR_927503.1:n.559T=
XR_927504.1:n.559T=
XR_001744842.2:n.586T=
XR_001744843.2:n.586T=
XR_002956472.1:n.586T=
XR_002956473.1:n.586T=
XR_002956474.1:n.586T=
XR_002956475.1:n.552T=
XR_002956476.1:n.552T=
XR_927494.3:n.586T=
XR_927500.3:n.586T=
XR_927503.3:n.586T=
NM_021167.5:c.304T= MANE Select NP_066990.3:p.Ser102=
NR_052016.2:n.552T=