Canonical Allele Identifier: CA2749263095

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27310126_27310127insTC , CM000664.2:g.27310126_27310127insTC	GRCh38
NC_000002.11:g.27532994_27532995insTC , CM000664.1:g.27532994_27532995insTC	GRCh37
NC_000002.10:g.27386498_27386499insTC	NCBI36
NG_008075.1:g.17437_17438insGA
NG_033055.1:g.3136_3137insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.462-146_462-145insGA MANE Select	ENSP00000369383.1:n.462-146_462-145insGA
ENST00000233545.6:c.462-146_462-145insGA	ENSP00000233545.2:n.462-146_462-145insGA
ENST00000357186.10:c.294-146_294-145insGA	ENSP00000349713.6:n.294-146_294-145insGA
ENST00000380044.5:c.462-146_462-145insGA	ENSP00000369383.1:n.462-146_462-145insGA
ENST00000402310.5:c.409-146_409-145insGA	ENSP00000383955.1:n.409-146_409-145insGA
ENST00000402722.5:c.*41-146_*41-145insGA	ENSP00000386000.1:n.*41-146_*41-145insGA
ENST00000405076.5:c.273-146_273-145insGA	ENSP00000385175.1:n.273-146_273-145insGA
ENST00000405983.5:c.507-146_507-145insGA	ENSP00000384586.1:n.507-146_507-145insGA
ENST00000415514.5:c.*263-146_*263-145insGA	ENSP00000388043.1:n.*263-146_*263-145insGA
ENST00000426513.6:c.*127-146_*127-145insGA	ENSP00000403824.2:n.*127-146_*127-145insGA
ENST00000430991.5:c.296-146_296-145insGA
ENST00000620797.4:n.135-146_135-145insGA
ENST00000621183.4:n.765-146_765-145insGA
NM_002437.4:c.462-146_462-145insGA	NP_002428.1:n.462-146_462-145insGA
XM_005264326.2:c.462-146_462-145insGA	XP_005264383.1:n.462-146_462-145insGA
XM_005264327.2:c.303-146_303-145insGA	XP_005264384.1:n.303-146_303-145insGA
XM_006712021.2:c.414-146_414-145insGA	XP_006712084.1:n.414-146_414-145insGA
XM_005264326.4:c.462-146_462-145insGA	XP_005264383.1:n.462-146_462-145insGA
XM_006712021.3:c.414-146_414-145insGA	XP_006712084.1:n.414-146_414-145insGA
XM_017004150.1:c.444-146_444-145insGA	XP_016859639.1:n.444-146_444-145insGA
XM_017004151.1:c.414-146_414-145insGA	XP_016859640.1:n.414-146_414-145insGA
XM_017004152.1:c.303-146_303-145insGA	XP_016859641.1:n.303-146_303-145insGA
XM_024452913.1:c.414-146_414-145insGA	XP_024308681.1:n.414-146_414-145insGA
NM_002437.5:c.462-146_462-145insGA MANE Select	NP_002428.1:n.462-146_462-145insGA