Canonical Allele Identifier: CA1538211569
Gene: SLC45A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33951338A= , CM000667.2:g.33951338A= GRCh38
NC_000005.9:g.33951443A= , CM000667.1:g.33951443A= GRCh37
NC_000005.8:g.33987200A= NCBI36
NG_011691.2:g.38338T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.1156+216T= MANE Select ENSP00000296589.4:n.1156+216T=
ENST00000296589.8:c.1156+216T= ENSP00000296589.4:n.1156+216T=
ENST00000382102.7:c.1156+216T= ENSP00000371534.3:n.1156+216T=
ENST00000510600.1:c.631+216T= ENSP00000424010.1:n.631+216T=
NM_001012509.3:c.1156+216T= NP_001012527.1:n.1156+216T=
NM_016180.4:c.1156+216T= NP_057264.3:n.1156+216T=
XM_011514051.1:c.754+216T= XP_011512353.1:n.754+216T=
XR_925620.1:n.1973+216T=
NM_016180.5:c.1156+216T= MANE Select NP_057264.4:n.1156+216T=
NM_001012509.4:c.1156+216T= NP_001012527.2:n.1156+216T=
Search 100 bp 5'
Search 100 bp 3'