Canonical Allele Identifier: CA2649558025

Gene: HMCN1

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186129951_186129954del , CM000663.2:g.186129951_186129954del	GRCh38
NC_000001.10:g.186099083_186099086del , CM000663.1:g.186099083_186099086del	GRCh37
NC_000001.9:g.184365706_184365709del	NCBI36
NG_011841.1:g.400401_400404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.12905-15_12905-12del MANE Select	ENSP00000271588.4:n.12905-15_12905-12del
ENST00000271588.8:c.12905-15_12905-12del	ENSP00000271588.4:n.12905-15_12905-12del
NM_031935.2:c.12905-15_12905-12del	NP_114141.2:n.12905-15_12905-12del
XM_011510037.1:c.12620-15_12620-12del	XP_011508339.1:n.12620-15_12620-12del
XM_011510038.1:c.12905-15_12905-12del	XP_011508340.1:n.12905-15_12905-12del
XM_011510039.1:c.12905-15_12905-12del	XP_011508341.1:n.12905-15_12905-12del
XM_011510038.3:c.12905-15_12905-12del	XP_011508340.1:n.12905-15_12905-12del
XM_017002437.1:c.10928-15_10928-12del	XP_016857926.1:n.10928-15_10928-12del
NM_031935.3:c.12905-15_12905-12del MANE Select	NP_114141.2:n.12905-15_12905-12del