Canonical Allele Identifier: CA8770947
Community Standard Title: NM_000154.2(GALK1):c.447G>A (p.Thr149=)
Gene: GALK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75763348C>T , CM000679.2:g.75763348C>T GRCh38
NC_000017.10:g.73759429C>T , CM000679.1:g.73759429C>T GRCh37
NC_000017.9:g.71271024C>T NCBI36
NG_008079.1:g.6852G>A
NG_008079.2:g.6852G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000154.2:c.447G>A MANE Select NP_000145.1:p.Thr149=
ENST00000588479.6:c.447G>A MANE Select ENSP00000465930.1:p.Thr149=
NM_000154.1:c.447G>A NP_000145.1:p.Thr149=
NM_001381985.1:c.447G>A NP_001368914.1:p.Thr149=
ENST00000225614.6:c.447G>A ENSP00000225614.1:p.Thr149=
ENST00000586244.1:c.*171G>A ENSP00000468288.1:n.*171G>A
ENST00000587707.1:c.201G>A ENSP00000468341.1:p.Thr67=
ENST00000587707.2:c.447G>A ENSP00000468341.2:p.Thr149=
ENST00000588479.5:c.447G>A ENSP00000465930.1:p.Thr149=
ENST00000592494.1:n.468G>A
ENST00000592997.6:c.447G>A ENSP00000464765.2:p.Thr149=