Canonical Allele Identifier: CA1240221576

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27322667_27322671delinsCCAGA , CM000664.2:g.27322667_27322671delinsCCAGA	GRCh38
NC_000002.11:g.27545534_27545538delinsCCAGA , CM000664.1:g.27545534_27545538delinsCCAGA	GRCh37
NC_000002.10:g.27399038_27399042delinsCCAGA	NCBI36
NG_008075.1:g.4894_4898delinsTCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.-5-149_-5-145delinsTCTGG MANE Select	ENSP00000369383.1:n.-5-149_-5-145delinsTCTGG
ENST00000357186.10:c.18+1762_18+1766delinsTCTGG	ENSP00000349713.6:n.18+1762_18+1766delinsTCTGG
ENST00000380044.5:c.-5-149_-5-145delinsTCTGG	ENSP00000369383.1:n.-5-149_-5-145delinsTCTGG
ENST00000399052.8:c.-5-149_-5-145delinsTCTGG	ENSP00000382006.4:n.-5-149_-5-145delinsTCTGG
ENST00000402310.5:c.-5-149_-5-145delinsTCTGG	ENSP00000383955.1:n.-5-149_-5-145delinsTCTGG
ENST00000402722.5:c.-5-149_-5-145delinsTCTGG	ENSP00000386000.1:n.-5-149_-5-145delinsTCTGG
ENST00000403262.6:c.-5-149_-5-145delinsTCTGG	ENSP00000385671.1:n.-5-149_-5-145delinsTCTGG
ENST00000405076.5:c.-5-149_-5-145delinsTCTGG	ENSP00000385175.1:n.-5-149_-5-145delinsTCTGG
ENST00000405983.5:c.-5-149_-5-145delinsTCTGG	ENSP00000384586.1:n.-5-149_-5-145delinsTCTGG
ENST00000415514.5:c.-5-149_-5-145delinsTCTGG	ENSP00000388043.1:n.-5-149_-5-145delinsTCTGG
ENST00000426513.6:c.-5-149_-5-145delinsTCTGG	ENSP00000403824.2:n.-5-149_-5-145delinsTCTGG
ENST00000428910.5:c.-207-149_-207-145delinsTCTGG	ENSP00000405235.1:n.-207-149_-207-145delinsTCTGG
ENST00000486898.1:n.47-149_47-145delinsTCTGG
ENST00000494436.1:n.27-149_27-145delinsTCTGG
ENST00000617583.4:n.22-149_22-145delinsTCTGG
ENST00000621183.4:n.52-149_52-145delinsTCTGG
ENST00000621470.4:n.47-149_47-145delinsTCTGG
ENST00000622003.4:n.12-149_12-145delinsTCTGG
NM_002437.4:c.-5-149_-5-145delinsTCTGG	NP_002428.1:n.-5-149_-5-145delinsTCTGG
XM_005264326.2:c.-5-149_-5-145delinsTCTGG	XP_005264383.1:n.-5-149_-5-145delinsTCTGG
XM_005264327.2:c.-129-149_-129-145delinsTCTGG	XP_005264384.1:n.-129-149_-129-145delinsTCTGG
XM_006712021.2:c.-210-149_-210-145delinsTCTGG	XP_006712084.1:n.-210-149_-210-145delinsTCTGG
XM_005264326.4:c.-5-149_-5-145delinsTCTGG	XP_005264383.1:n.-5-149_-5-145delinsTCTGG
XM_006712021.3:c.-210-149_-210-145delinsTCTGG	XP_006712084.1:n.-210-149_-210-145delinsTCTGG
XM_017004150.1:c.-3257-149_-3257-145delinsTCTGG	XP_016859639.1:n.-3257-149_-3257-145delinsTCTGG
XM_024452913.1:c.-210-149_-210-145delinsTCTGG	XP_024308681.1:n.-210-149_-210-145delinsTCTGG
NM_002437.5:c.-5-149_-5-145delinsTCTGG MANE Select	NP_002428.1:n.-5-149_-5-145delinsTCTGG