Canonical Allele Identifier: CA1748577
Community Standard Title: NM_016622.4(MRPL35):c.428G>A (p.Arg143Gln)
Gene: MRPL35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.86210529G>A , CM000664.2:g.86210529G>A GRCh38
NC_000002.11:g.86437652G>A , CM000664.1:g.86437652G>A GRCh37
NC_000002.10:g.86291163G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_016622.4:c.428G>A MANE Select NP_057706.2:p.Arg143Gln
ENST00000337109.9:c.428G>A MANE Select ENSP00000338389.4:p.Arg143Gln
NM_001363782.1:c.428G>A NP_001350711.1:p.Arg143Gln
NM_016622.3:c.428G>A NP_057706.2:p.Arg143Gln
NM_145644.2:c.428G>A NP_663619.1:p.Arg143Gln
NM_145644.3:c.428G>A NP_663619.1:p.Arg143Gln
ENST00000254644.12:c.428G>A ENSP00000254644.7:p.Arg143Gln
ENST00000337109.8:c.428G>A ENSP00000338389.4:p.Arg143Gln
ENST00000409180.1:c.428G>A ENSP00000386255.1:p.Arg143Gln
ENST00000605125.5:c.283G>A ENSP00000473925.1:p.Asp95Asn
XM_005264361.2:c.428G>A XP_005264418.1:p.Arg143Gln