Canonical Allele Identifier: CA2692135136
Gene: HMCN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130433123_130433124del , CM000671.2:g.130433123_130433124del GRCh38
NC_000009.11:g.133308510_133308511del , CM000671.1:g.133308510_133308511del GRCh37
NC_000009.10:g.132298331_132298332del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624552.4:c.14838-225_14838-224del ENSP00000485357.2:n.14838-225_14838-224del
ENST00000683500.2:c.14895-225_14895-224del MANE Select ENSP00000508292.2:n.14895-225_14895-224del
ENST00000623487.1:n.3016_3017del
ENST00000624552.3:c.14835-225_14835-224del ENSP00000485357.1:n.14835-225_14835-224del
NM_001291815.1:c.14895-225_14895-224del NP_001278744.1:n.14895-225_14895-224del
XM_011518465.1:c.14772-225_14772-224del XP_011516767.1:n.14772-225_14772-224del
XM_011518466.1:c.14763-225_14763-224del XP_011516768.1:n.14763-225_14763-224del
XM_011518467.1:c.14718-225_14718-224del XP_011516769.1:n.14718-225_14718-224del
NM_001291815.2:c.14895-225_14895-224del MANE Select NP_001278744.1:n.14895-225_14895-224del
XM_011518465.2:c.14772-225_14772-224del XP_011516767.1:n.14772-225_14772-224del
XM_011518466.2:c.14763-225_14763-224del XP_011516768.1:n.14763-225_14763-224del
XM_011518467.2:c.14718-225_14718-224del XP_011516769.1:n.14718-225_14718-224del
XM_017014585.1:c.11676-225_11676-224del XP_016870074.1:n.11676-225_11676-224del
XM_017014586.1:c.7473-225_7473-224del XP_016870075.1:n.7473-225_7473-224del
XR_001746957.1:n.92+497_92+498del
XR_001746958.1:n.92+497_92+498del