Canonical Allele Identifier: CA365766542

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219288A>G (hg19) ; chr6:g.136898150A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898150A>G , CM000668.2:g.136898150A>G	GRCh38
NC_000006.11:g.137219288A>G , CM000668.1:g.137219288A>G	GRCh37
NC_000006.10:g.137260981A>G	NCBI36
NG_008462.1:g.80571A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.812A>G MANE Select	ENSP00000315680.3:p.Asn271Ser
ENST00000541292.6:c.*77A>G	ENSP00000441004.1:n.*77A>G
ENST00000678002.1:c.500A>G
ENST00000678557.1:c.698A>G	ENSP00000502962.1:p.Asn233Ser
ENST00000679286.1:c.692A>G	ENSP00000503168.1:p.Asn231Ser
ENST00000318471.4:c.812A>G	ENSP00000315680.3:p.Asn271Ser
NM_000288.3:c.812A>G	NP_000279.1:p.Asn271Ser
XM_005267019.3:c.698A>G	XP_005267076.1:p.Asn233Ser
XM_006715502.1:c.518A>G	XP_006715565.1:p.Asn173Ser
XM_011535900.1:c.535A>G	XP_011534202.1:p.Thr179Ala
XM_005267019.4:c.698A>G	XP_005267076.1:p.Asn233Ser
XM_006715502.2:c.518A>G	XP_006715565.1:p.Asn173Ser
XM_017010934.2:c.535A>G	XP_016866423.1:p.Thr179Ala
NM_000288.4:c.812A>G MANE Select	NP_000279.1:p.Asn271Ser