Canonical Allele Identifier: CA1626000487

Gene: SLC25A27

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.46657898C= , CM000668.2:g.46657898C=	GRCh38
NC_000006.11:g.46625635C= , CM000668.1:g.46625635C=	GRCh37
NC_000006.10:g.46733594C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004277.5:c.299-1064C= MANE Select	NP_004268.3:n.299-1064C=
ENST00000371347.10:c.299-1064C= MANE Select	ENSP00000360398.3:n.299-1064C=
NM_001204051.1:c.299-1064C=	NP_001190980.1:n.299-1064C=
NM_001204051.2:c.299-1064C=	NP_001190980.1:n.299-1064C=
NM_001204052.1:c.299-1064C=	NP_001190981.1:n.299-1064C=
NM_001204052.2:c.299-1064C=	NP_001190981.1:n.299-1064C=
NM_004277.4:c.299-1064C=	NP_004268.3:n.299-1064C=
ENST00000371347.9:c.299-1064C=	ENSP00000360398.3:n.299-1064C=
ENST00000411689.6:c.299-1064C=	ENSP00000412024.2:n.299-1064C=
XM_005249483.2:c.299-1064C=	XP_005249540.1:n.299-1064C=
XM_005249485.1:c.-17-1064C=	XP_005249542.1:n.-17-1064C=
XR_427858.1:n.547-1064C=