Canonical Allele Identifier: CA1240217138

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312600_27312605delinsGAAATT , CM000664.2:g.27312600_27312605delinsGAAATT	GRCh38
NC_000002.11:g.27535467_27535472delinsGAAATT , CM000664.1:g.27535467_27535472delinsGAAATT	GRCh37
NC_000002.10:g.27388971_27388976delinsGAAATT	NCBI36
NG_008075.1:g.14960_14965delinsAATTTC
NG_033055.1:g.659_664delinsAATTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.280-16_280-11delinsAATTTC MANE Select	ENSP00000369383.1:n.280-16_280-11delinsAATTTC
ENST00000233545.6:c.280-16_280-11delinsAATTTC	ENSP00000233545.2:n.280-16_280-11delinsAATTTC
ENST00000357186.10:c.112-16_112-11delinsAATTTC	ENSP00000349713.6:n.112-16_112-11delinsAATTTC
ENST00000380044.5:c.280-16_280-11delinsAATTTC	ENSP00000369383.1:n.280-16_280-11delinsAATTTC
ENST00000402310.5:c.280-16_280-11delinsAATTTC	ENSP00000383955.1:n.280-16_280-11delinsAATTTC
ENST00000402722.5:c.245-16_245-11delinsAATTTC	ENSP00000386000.1:n.245-16_245-11delinsAATTTC
ENST00000403262.6:c.280-16_280-11delinsAATTTC	ENSP00000385671.1:n.280-16_280-11delinsAATTTC
ENST00000405076.5:c.187-359_187-354delinsAATTTC	ENSP00000385175.1:n.187-359_187-354delinsAATTTC
ENST00000405983.5:c.325-16_325-11delinsAATTTC	ENSP00000384586.1:n.325-16_325-11delinsAATTTC
ENST00000415514.5:c.*81-16_*81-11delinsAATTTC	ENSP00000388043.1:n.*81-16_*81-11delinsAATTTC
ENST00000426513.6:c.245-16_245-11delinsAATTTC	ENSP00000403824.2:n.245-16_245-11delinsAATTTC
ENST00000428910.5:c.202-16_202-11delinsAATTTC	ENSP00000405235.1:n.202-16_202-11delinsAATTTC
ENST00000430991.5:c.209+75_209+80delinsAATTTC
ENST00000475085.1:n.308-16_308-11delinsAATTTC
ENST00000616446.1:n.257-16_257-11delinsAATTTC
ENST00000616707.1:n.783_788delinsAATTTC
ENST00000617583.4:n.306-16_306-11delinsAATTTC
ENST00000621183.4:n.336-16_336-11delinsAATTTC
ENST00000621470.4:n.296-16_296-11delinsAATTTC
ENST00000622003.4:n.453-16_453-11delinsAATTTC
NM_002437.4:c.280-16_280-11delinsAATTTC	NP_002428.1:n.280-16_280-11delinsAATTTC
XM_005264326.2:c.280-16_280-11delinsAATTTC	XP_005264383.1:n.280-16_280-11delinsAATTTC
XM_005264327.2:c.121-16_121-11delinsAATTTC	XP_005264384.1:n.121-16_121-11delinsAATTTC
XM_006712021.2:c.232-16_232-11delinsAATTTC	XP_006712084.1:n.232-16_232-11delinsAATTTC
XM_005264326.4:c.280-16_280-11delinsAATTTC	XP_005264383.1:n.280-16_280-11delinsAATTTC
XM_006712021.3:c.232-16_232-11delinsAATTTC	XP_006712084.1:n.232-16_232-11delinsAATTTC
XM_017004150.1:c.262-16_262-11delinsAATTTC	XP_016859639.1:n.262-16_262-11delinsAATTTC
XM_017004151.1:c.232-16_232-11delinsAATTTC	XP_016859640.1:n.232-16_232-11delinsAATTTC
XM_017004152.1:c.121-16_121-11delinsAATTTC	XP_016859641.1:n.121-16_121-11delinsAATTTC
XM_024452913.1:c.232-16_232-11delinsAATTTC	XP_024308681.1:n.232-16_232-11delinsAATTTC
NM_002437.5:c.280-16_280-11delinsAATTTC MANE Select	NP_002428.1:n.280-16_280-11delinsAATTTC