Canonical Allele Identifier: CA365766592

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219306C>A (hg19) ; chr6:g.136898168C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898168C>A , CM000668.2:g.136898168C>A	GRCh38
NC_000006.11:g.137219306C>A , CM000668.1:g.137219306C>A	GRCh37
NC_000006.10:g.137260999C>A	NCBI36
NG_008462.1:g.80589C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.830C>A MANE Select	ENSP00000315680.3:p.Ser277Tyr
ENST00000541292.6:c.*95C>A	ENSP00000441004.1:n.*95C>A
ENST00000678002.1:c.518C>A
ENST00000678557.1:c.716C>A	ENSP00000502962.1:p.Ser239Tyr
ENST00000679286.1:c.710C>A	ENSP00000503168.1:p.Ser237Tyr
ENST00000318471.4:c.830C>A	ENSP00000315680.3:p.Ser277Tyr
NM_000288.3:c.830C>A	NP_000279.1:p.Ser277Tyr
XM_005267019.3:c.716C>A	XP_005267076.1:p.Ser239Tyr
XM_006715502.1:c.536C>A	XP_006715565.1:p.Ser179Tyr
XM_011535900.1:c.553C>A	XP_011534202.1:p.Leu185Ile
XM_005267019.4:c.716C>A	XP_005267076.1:p.Ser239Tyr
XM_006715502.2:c.536C>A	XP_006715565.1:p.Ser179Tyr
XM_017010934.2:c.553C>A	XP_016866423.1:p.Leu185Ile
NM_000288.4:c.830C>A MANE Select	NP_000279.1:p.Ser277Tyr