Canonical Allele Identifier: CA1212846639

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185734748_185734760delinsTGAGGGGGAAAAA , CM000663.2:g.185734748_185734760delinsTGAGGGGGAAAAA	GRCh38
NC_000001.10:g.185703880_185703892delinsTGAGGGGGAAAAA , CM000663.1:g.185703880_185703892delinsTGAGGGGGAAAAA	GRCh37
NC_000001.9:g.183970503_183970515delinsTGAGGGGGAAAAA	NCBI36
NG_011841.1:g.5198_5210delinsTGAGGGGGAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.-32_-20delinsTGAGGGGGAAAAA MANE Select	ENSP00000271588.4:n.-32_-20delinsTGAGGGGGAAAAA
ENST00000271588.8:c.-32_-20delinsTGAGGGGGAAAAA	ENSP00000271588.4:n.-32_-20delinsTGAGGGGGAAAAA
NM_031935.2:c.-32_-20delinsTGAGGGGGAAAAA	NP_114141.2:n.-32_-20delinsTGAGGGGGAAAAA
XM_011510037.1:c.-32_-20delinsTGAGGGGGAAAAA	XP_011508339.1:n.-32_-20delinsTGAGGGGGAAAAA
XM_011510038.1:c.-32_-20delinsTGAGGGGGAAAAA	XP_011508340.1:n.-32_-20delinsTGAGGGGGAAAAA
XM_011510039.1:c.-32_-20delinsTGAGGGGGAAAAA	XP_011508341.1:n.-32_-20delinsTGAGGGGGAAAAA
XM_011510040.1:c.-32_-20delinsTGAGGGGGAAAAA	XP_011508342.1:n.-32_-20delinsTGAGGGGGAAAAA
XM_011510041.1:c.-32_-20delinsTGAGGGGGAAAAA	XP_011508343.1:n.-32_-20delinsTGAGGGGGAAAAA
XM_011510038.3:c.-32_-20delinsTGAGGGGGAAAAA	XP_011508340.1:n.-32_-20delinsTGAGGGGGAAAAA
XM_011510041.3:c.-32_-20delinsTGAGGGGGAAAAA	XP_011508343.1:n.-32_-20delinsTGAGGGGGAAAAA
XM_024450118.1:c.-32_-20delinsTGAGGGGGAAAAA	XP_024305886.1:n.-32_-20delinsTGAGGGGGAAAAA
NM_031935.3:c.-32_-20delinsTGAGGGGGAAAAA MANE Select	NP_114141.2:n.-32_-20delinsTGAGGGGGAAAAA