Canonical Allele Identifier: CA1152270645

Gene: SLC45A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8325962A= , CM000663.2:g.8325962A=	GRCh38
NC_000001.10:g.8386022A= , CM000663.1:g.8386022A=	GRCh37
NC_000001.9:g.8308609A=	NCBI36
NG_034025.1:g.12878A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000471889.7:c.635A= MANE Select	ENSP00000418096.3:p.Asn212=
ENST00000289877.8:c.635A=	ENSP00000289877.8:p.Asn212=
ENST00000471889.5:c.737A=	ENSP00000418096.2:p.Asn246=
NM_001080397.2:c.737A=	NP_001073866.2:p.Asn246=
XM_011541530.1:c.737A=	XP_011539832.1:p.Asn246=
XM_011541531.1:c.644A=	XP_011539833.1:p.Asn215=
XM_011541530.2:c.737A=	XP_011539832.1:p.Asn246=
XM_011541531.2:c.644A=	XP_011539833.1:p.Asn215=
XM_024447371.1:c.644A=	XP_024303139.1:p.Asn215=
XM_024447372.1:c.29A=	XP_024303140.1:p.Asn10=
NM_001080397.3:c.635A= MANE Select	NP_001073866.3:p.Asn212=
NM_001379614.1:c.635A=	NP_001366543.1:p.Asn212=
NM_001379615.1:c.542A=	NP_001366544.1:p.Asn181=
NM_001379616.1:c.542A=	NP_001366545.1:p.Asn181=
NM_001379617.1:c.29A=	NP_001366546.1:p.Asn10=
NM_001379618.1:c.29A=	NP_001366547.1:p.Asn10=