Canonical Allele Identifier: CA1294491

Gene: HMCN1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186129948_186129950del , CM000663.2:g.186129948_186129950del	GRCh38
NC_000001.10:g.186099080_186099082del , CM000663.1:g.186099080_186099082del	GRCh37
NC_000001.9:g.184365703_184365705del	NCBI36
NG_011841.1:g.400398_400400del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.12905-18_12905-16del MANE Select	ENSP00000271588.4:n.12905-18_12905-16del
ENST00000271588.8:c.12905-18_12905-16del	ENSP00000271588.4:n.12905-18_12905-16del
NM_031935.2:c.12905-18_12905-16del	NP_114141.2:n.12905-18_12905-16del
XM_011510037.1:c.12620-18_12620-16del	XP_011508339.1:n.12620-18_12620-16del
XM_011510038.1:c.12905-18_12905-16del	XP_011508340.1:n.12905-18_12905-16del
XM_011510039.1:c.12905-18_12905-16del	XP_011508341.1:n.12905-18_12905-16del
XM_011510038.3:c.12905-18_12905-16del	XP_011508340.1:n.12905-18_12905-16del
XM_017002437.1:c.10928-18_10928-16del	XP_016857926.1:n.10928-18_10928-16del
NM_031935.3:c.12905-18_12905-16del MANE Select	NP_114141.2:n.12905-18_12905-16del