Canonical Allele Identifier: CA10479636

Gene: SLC25A53 ZCCHC18

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.104114119G>C , CM000685.2:g.104114119G>C	GRCh38
NC_000023.10:g.103358810G>C , CM000685.1:g.103358810G>C	GRCh37
NC_000023.9:g.103245466G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594199.3:c.-31-8831C>G (SLC25A53) MANE Select	ENSP00000468980.1:n.-31-8831C>G
ENST00000650639.1:c.8G>C (ZCCHC18) MANE Select	ENSP00000498828.1:p.Ser3Thr
ENST00000422784.5:n.650+546G>C (ZCCHC18)
ENST00000537356.3:c.8G>C (ZCCHC18)	ENSP00000473824.1:p.Ser3Thr
ENST00000594199.2:c.-31-8831C>G (SLC25A53)	ENSP00000468980.1:n.-31-8831C>G
ENST00000611638.4:c.8G>C (ZCCHC18)	ENSP00000482195.1:p.Ser3Thr
NM_001012755.4:c.-31-8831C>G (SLC25A53)	NP_001012773.2:n.-31-8831C>G
NM_001143978.2:c.8G>C (ZCCHC18)	NP_001137450.1:p.Ser3Thr
NR_026694.2:n.668+546G>C (ZCCHC18)
XM_011531012.1:c.8G>C (ZCCHC18)	XP_011529314.1:p.Ser3Thr
XM_011531012.3:c.8G>C (ZCCHC18)	XP_011529314.1:p.Ser3Thr
NM_001012755.5:c.-31-8831C>G (SLC25A53) MANE Select	NP_001012773.2:n.-31-8831C>G
NM_001143978.3:c.8G>C (ZCCHC18) MANE Select	NP_001137450.1:p.Ser3Thr
NR_026694.3:n.671+546G>C (ZCCHC18)