Canonical Allele Identifier: CA1212846651

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185734766_185734769delinsGGAA , CM000663.2:g.185734766_185734769delinsGGAA	GRCh38
NC_000001.10:g.185703898_185703901delinsGGAA , CM000663.1:g.185703898_185703901delinsGGAA	GRCh37
NC_000001.9:g.183970521_183970524delinsGGAA	NCBI36
NG_011841.1:g.5216_5219delinsGGAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000271588.9:c.-14_-11delinsGGAA MANE Select	ENSP00000271588.4:n.-14_-11delinsGGAA
ENST00000271588.8:c.-14_-11delinsGGAA	ENSP00000271588.4:n.-14_-11delinsGGAA
NM_031935.2:c.-14_-11delinsGGAA	NP_114141.2:n.-14_-11delinsGGAA
XM_011510037.1:c.-14_-11delinsGGAA	XP_011508339.1:n.-14_-11delinsGGAA
XM_011510038.1:c.-14_-11delinsGGAA	XP_011508340.1:n.-14_-11delinsGGAA
XM_011510039.1:c.-14_-11delinsGGAA	XP_011508341.1:n.-14_-11delinsGGAA
XM_011510040.1:c.-14_-11delinsGGAA	XP_011508342.1:n.-14_-11delinsGGAA
XM_011510041.1:c.-14_-11delinsGGAA	XP_011508343.1:n.-14_-11delinsGGAA
XM_011510038.3:c.-14_-11delinsGGAA	XP_011508340.1:n.-14_-11delinsGGAA
XM_011510041.3:c.-14_-11delinsGGAA	XP_011508343.1:n.-14_-11delinsGGAA
XM_024450118.1:c.-14_-11delinsGGAA	XP_024305886.1:n.-14_-11delinsGGAA
NM_031935.3:c.-14_-11delinsGGAA MANE Select	NP_114141.2:n.-14_-11delinsGGAA