Canonical Allele Identifier: CA365766521

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219280A>C (hg19) ; chr6:g.136898142A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898142A>C , CM000668.2:g.136898142A>C	GRCh38
NC_000006.11:g.137219280A>C , CM000668.1:g.137219280A>C	GRCh37
NC_000006.10:g.137260973A>C	NCBI36
NG_008462.1:g.80563A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.804A>C MANE Select	ENSP00000315680.3:p.Arg268Ser
ENST00000541292.6:c.*69A>C	ENSP00000441004.1:n.*69A>C
ENST00000678002.1:c.492A>C
ENST00000678557.1:c.690A>C	ENSP00000502962.1:p.Arg230Ser
ENST00000679286.1:c.684A>C	ENSP00000503168.1:p.Arg228Ser
ENST00000318471.4:c.804A>C	ENSP00000315680.3:p.Arg268Ser
NM_000288.3:c.804A>C	NP_000279.1:p.Arg268Ser
XM_005267019.3:c.690A>C	XP_005267076.1:p.Arg230Ser
XM_006715502.1:c.510A>C	XP_006715565.1:p.Arg170Ser
XM_011535900.1:c.527A>C	XP_011534202.1:p.Asp176Ala
XM_005267019.4:c.690A>C	XP_005267076.1:p.Arg230Ser
XM_006715502.2:c.510A>C	XP_006715565.1:p.Arg170Ser
XM_017010934.2:c.527A>C	XP_016866423.1:p.Asp176Ala
NM_000288.4:c.804A>C MANE Select	NP_000279.1:p.Arg268Ser