Canonical Allele Identifier: CA365764158

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137191140A>C (hg19) ; chr6:g.136870002A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136870002A>C , CM000668.2:g.136870002A>C	GRCh38
NC_000006.11:g.137191140A>C , CM000668.1:g.137191140A>C	GRCh37
NC_000006.10:g.137232833A>C	NCBI36
NG_008462.1:g.52423A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.746A>C MANE Select	ENSP00000315680.3:p.Lys249Thr
ENST00000541292.6:c.746A>C	ENSP00000441004.1:p.Lys249Thr
ENST00000678002.1:c.434A>C
ENST00000678557.1:c.632A>C	ENSP00000502962.1:p.Lys211Thr
ENST00000678593.1:c.751A>C	ENSP00000503841.1:n.751A>C
ENST00000679286.1:c.626A>C	ENSP00000503168.1:p.Lys209Thr
ENST00000318471.4:c.746A>C	ENSP00000315680.3:p.Lys249Thr
ENST00000541292.5:c.746A>C	ENSP00000441004.1:p.Lys249Thr
NM_000288.3:c.746A>C	NP_000279.1:p.Lys249Thr
XM_005267019.3:c.632A>C	XP_005267076.1:p.Lys211Thr
XM_006715502.1:c.452A>C	XP_006715565.1:p.Lys151Thr
XM_011535900.1:c.526+23821A>C	XP_011534202.1:n.526+23821A>C
XM_005267019.4:c.632A>C	XP_005267076.1:p.Lys211Thr
XM_006715502.2:c.452A>C	XP_006715565.1:p.Lys151Thr
XM_017010934.2:c.526+23821A>C	XP_016866423.1:n.526+23821A>C
NM_000288.4:c.746A>C MANE Select	NP_000279.1:p.Lys249Thr