Canonical Allele Identifier: CA427118684
Gene: SUCLG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.84652605A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.84425481A>T , CM000664.2:g.84425481A>T GRCh38
NC_000002.11:g.84652605A>T , CM000664.1:g.84652605A>T GRCh37
NC_000002.10:g.84506116A>T NCBI36
NG_016755.1:g.38982T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000393868.7:c.948T>A MANE Select ENSP00000377446.2:p.Ser316=
ENST00000651342.1:c.*388T>A ENSP00000498471.1:n.*388T>A
ENST00000393868.6:c.948T>A ENSP00000377446.2:p.Ser316=
ENST00000484365.1:n.1456T>A
ENST00000487809.1:n.695T>A
ENST00000491123.5:n.794T>A
NM_003849.3:c.948T>A NP_003840.2:p.Ser316=
NM_003849.4:c.948T>A MANE Select NP_003840.2:p.Ser316=