Canonical Allele Identifier: CA2649555643
Gene: HMCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186082783_186082784dup , CM000663.2:g.186082783_186082784dup GRCh38
NC_000001.10:g.186051915_186051916dup , CM000663.1:g.186051915_186051916dup GRCh37
NC_000001.9:g.184318538_184318539dup NCBI36
NG_011841.1:g.353233_353234dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.8788-82_8788-81dup MANE Select ENSP00000271588.4:n.8788-82_8788-81dup
ENST00000271588.8:c.8788-82_8788-81dup ENSP00000271588.4:n.8788-82_8788-81dup
NM_031935.2:c.8788-82_8788-81dup NP_114141.2:n.8788-82_8788-81dup
XM_011510037.1:c.8788-82_8788-81dup XP_011508339.1:n.8788-82_8788-81dup
XM_011510038.1:c.8788-82_8788-81dup XP_011508340.1:n.8788-82_8788-81dup
XM_011510039.1:c.8788-82_8788-81dup XP_011508341.1:n.8788-82_8788-81dup
XM_011510040.1:c.8788-82_8788-81dup XP_011508342.1:n.8788-82_8788-81dup
XM_011510041.1:c.8788-82_8788-81dup XP_011508343.1:n.8788-82_8788-81dup
XM_011510038.3:c.8788-82_8788-81dup XP_011508340.1:n.8788-82_8788-81dup
XM_011510041.3:c.8788-82_8788-81dup XP_011508343.1:n.8788-82_8788-81dup
XM_017002437.1:c.6811-82_6811-81dup XP_016857926.1:n.6811-82_6811-81dup
XM_024450118.1:c.8788-82_8788-81dup XP_024305886.1:n.8788-82_8788-81dup
NM_031935.3:c.8788-82_8788-81dup MANE Select NP_114141.2:n.8788-82_8788-81dup
Search 100 bp 5'
Search 100 bp 3'