Canonical Allele Identifier: CA1197524
Community Standard Title: NM_002857.4(PEX19):c.-4C>T
Gene: PEX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160285128G>A , CM000663.2:g.160285128G>A GRCh38
NC_000001.10:g.160254918G>A , CM000663.1:g.160254918G>A GRCh37
NC_000001.9:g.158521542G>A NCBI36
NG_008637.1:g.5024C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002857.4:c.-4C>T MANE Select NP_002848.1:n.-4C>T
ENST00000368072.10:c.-4C>T MANE Select ENSP00000357051.5:n.-4C>T
NM_001193644.1:c.-4C>T NP_001180573.1:n.-4C>T
NM_002857.3:c.-4C>T NP_002848.1:n.-4C>T
NR_036492.1:n.24C>T
NR_036492.2:n.6C>T
NR_036493.1:n.24C>T
NR_036493.2:n.6C>T
ENST00000368072.9:c.-4C>T ENSP00000357051.5:n.-4C>T
ENST00000472750.5:c.-4C>T ENSP00000434633.1:n.-4C>T
ENST00000524939.1:n.14C>T
ENST00000532643.5:c.-4C>T ENSP00000435915.1:n.-4C>T
ENST00000533104.1:n.6C>T
ENST00000533699.5:n.64+1157C>T
ENST00000556710.5:c.-249C>T ENSP00000451235.1:n.-249C>T
ENST00000556710.6:c.-4C>T ENSP00000451235.2:n.-4C>T
XR_001738265.1:n.88+273G>A