Canonical Allele Identifier: CA2773213236

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136826508_136826509insA , CM000668.2:g.136826508_136826509insA	GRCh38
NC_000006.11:g.137147646_137147647insA , CM000668.1:g.137147646_137147647insA	GRCh37
NC_000006.10:g.137189339_137189340insA	NCBI36
NG_008462.1:g.8929_8930insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.339+39_339+40insA MANE Select	ENSP00000315680.3:n.339+39_339+40insA
ENST00000541292.6:c.339+39_339+40insA	ENSP00000441004.1:n.339+39_339+40insA
ENST00000678002.1:c.214+39_214+40insA
ENST00000678557.1:c.225+39_225+40insA	ENSP00000502962.1:n.225+39_225+40insA
ENST00000678593.1:c.344+39_344+40insA	ENSP00000503841.1:n.344+39_344+40insA
ENST00000679286.1:c.219+39_219+40insA	ENSP00000503168.1:n.219+39_219+40insA
ENST00000318471.4:c.339+39_339+40insA	ENSP00000315680.3:n.339+39_339+40insA
ENST00000367756.8:c.339+39_339+40insA	ENSP00000356730.4:n.339+39_339+40insA
ENST00000541292.5:c.339+39_339+40insA	ENSP00000441004.1:n.339+39_339+40insA
NM_000288.3:c.339+39_339+40insA	NP_000279.1:n.339+39_339+40insA
XM_005267019.3:c.225+39_225+40insA	XP_005267076.1:n.225+39_225+40insA
XM_006715502.1:c.339+39_339+40insA	XP_006715565.1:n.339+39_339+40insA
XM_011535900.1:c.339+39_339+40insA	XP_011534202.1:n.339+39_339+40insA
XM_005267019.4:c.225+39_225+40insA	XP_005267076.1:n.225+39_225+40insA
XM_006715502.2:c.339+39_339+40insA	XP_006715565.1:n.339+39_339+40insA
XM_017010934.2:c.339+39_339+40insA	XP_016866423.1:n.339+39_339+40insA
NM_000288.4:c.339+39_339+40insA MANE Select	NP_000279.1:n.339+39_339+40insA