Canonical Allele Identifier: CA365766595

Gene: PEX7

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.830C>T MANE Select	ENSP00000315680.3:p.Ser277Phe
ENST00000541292.6:c.*95C>T	ENSP00000441004.1:n.*95C>T
ENST00000678002.1:c.518C>T
ENST00000678557.1:c.716C>T	ENSP00000502962.1:p.Ser239Phe
ENST00000679286.1:c.710C>T	ENSP00000503168.1:p.Ser237Phe
ENST00000318471.4:c.830C>T	ENSP00000315680.3:p.Ser277Phe
NM_000288.3:c.830C>T	NP_000279.1:p.Ser277Phe
XM_005267019.3:c.716C>T	XP_005267076.1:p.Ser239Phe
XM_006715502.1:c.536C>T	XP_006715565.1:p.Ser179Phe
XM_011535900.1:c.553C>T	XP_011534202.1:p.Leu185Phe
XM_005267019.4:c.716C>T	XP_005267076.1:p.Ser239Phe
XM_006715502.2:c.536C>T	XP_006715565.1:p.Ser179Phe
XM_017010934.2:c.553C>T	XP_016866423.1:p.Leu185Phe
NM_000288.4:c.830C>T MANE Select	NP_000279.1:p.Ser277Phe