Canonical Allele Identifier: CA1197197

Gene: PEX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160279582C>G , CM000663.2:g.160279582C>G	GRCh38
NC_000001.10:g.160249372C>G , CM000663.1:g.160249372C>G	GRCh37
NC_000001.9:g.158515996C>G	NCBI36
NG_008637.1:g.10570G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002857.4:c.869G>C MANE Select	NP_002848.1:p.Gly290Ala
ENST00000368072.10:c.869G>C MANE Select	ENSP00000357051.5:p.Gly290Ala
NM_001193644.1:c.817G>C	NP_001180573.1:p.Val273Leu
NM_002857.3:c.869G>C	NP_002848.1:p.Gly290Ala
NR_036492.1:n.786G>C
NR_036492.2:n.768G>C
NR_036493.1:n.810G>C
NR_036493.2:n.792G>C
ENST00000368072.9:c.869G>C	ENSP00000357051.5:p.Gly290Ala
ENST00000462644.5:c.*222G>C	ENSP00000435896.1:n.*222G>C
ENST00000467711.5:n.58+219G>C
ENST00000472750.5:c.*636G>C	ENSP00000434633.1:n.*636G>C
ENST00000485079.1:c.426+219G>C	ENSP00000450870.1:n.426+219G>C
ENST00000495624.1:c.547G>C
ENST00000532508.5:n.951G>C
ENST00000532643.5:c.*222G>C	ENSP00000435915.1:n.*222G>C
ENST00000556710.5:c.375+219G>C	ENSP00000451235.1:n.375+219G>C
ENST00000556710.6:c.*497+219G>C	ENSP00000451235.2:n.*497+219G>C
ENST00000647676.1:c.114+219G>C	ENSP00000497162.1:n.114+219G>C