Canonical Allele Identifier: CA1807209021

Gene: SLC25A32

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.103400160C= , CM000670.2:g.103400160C=	GRCh38
NC_000008.10:g.104412388C= , CM000670.1:g.104412388C=	GRCh37
NC_000008.9:g.104481564C=	NCBI36
NG_047200.1:g.20176G=

Transcript Alleles

HGVS	Amino-acid Change
NM_030780.5:c.*251G= MANE Select	NP_110407.2:n.*251G=
ENST00000297578.9:c.*251G= MANE Select	ENSP00000297578.4:n.*251G=
NM_030780.4:c.*251G=	NP_110407.2:n.*251G=
NR_102337.1:n.1511G=
NR_102337.2:n.1283G=
NR_102338.1:n.1706G=
NR_102338.2:n.1478G=
ENST00000297578.8:c.*251G=	ENSP00000297578.4:n.*251G=
ENST00000521645.5:c.*588G=	ENSP00000430989.1:n.*588G=
ENST00000523256.6:c.*580G=	ENSP00000427737.1:n.*580G=
ENST00000523866.1:c.*741G=	ENSP00000430371.1:n.*741G=
ENST00000649416.1:c.*251G=	ENSP00000496817.1:n.*251G=
ENST00000707124.1:c.*251G=	ENSP00000516752.1:n.*251G=