Canonical Allele Identifier: CA343264213

Gene: PEX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160283529C>A , CM000663.2:g.160283529C>A	GRCh38
NC_000001.10:g.160253319C>A , CM000663.1:g.160253319C>A	GRCh37
NC_000001.9:g.158519943C>A	NCBI36
NG_008637.1:g.6623G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002857.4:c.180+1G>T MANE Select	NP_002848.1:n.180+1G>T
ENST00000368072.10:c.180+1G>T MANE Select	ENSP00000357051.5:n.180+1G>T
NM_001193644.1:c.180+1G>T	NP_001180573.1:n.180+1G>T
NM_002857.3:c.180+1G>T	NP_002848.1:n.180+1G>T
NR_036492.1:n.98-420G>T
NR_036492.2:n.80-420G>T
NR_036493.1:n.207+1G>T
NR_036493.2:n.189+1G>T
ENST00000368072.9:c.180+1G>T	ENSP00000357051.5:n.180+1G>T
ENST00000392220.2:c.120+1G>T	ENSP00000376054.2:n.120+1G>T
ENST00000462644.5:c.120+1G>T	ENSP00000435896.1:n.120+1G>T
ENST00000472750.5:c.71-420G>T	ENSP00000434633.1:n.71-420G>T
ENST00000524939.1:n.197+1G>T
ENST00000532508.5:n.152+1G>T
ENST00000532643.5:c.180+1G>T	ENSP00000435915.1:n.180+1G>T
ENST00000533104.1:n.80-420G>T
ENST00000533699.5:n.174+1G>T
ENST00000556710.5:c.-175-420G>T	ENSP00000451235.1:n.-175-420G>T
ENST00000556710.6:c.71-420G>T	ENSP00000451235.2:n.71-420G>T