Canonical Allele Identifier: CA2692135170
Gene: HMCN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130433147_130433148insGTTGAA , CM000671.2:g.130433147_130433148insGTTGAA GRCh38
NC_000009.11:g.133308534_133308535insGTTGAA , CM000671.1:g.133308534_133308535insGTTGAA GRCh37
NC_000009.10:g.132298355_132298356insGTTGAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624552.4:c.14838-201_14838-200insGTTGAA ENSP00000485357.2:n.14838-201_14838-200insGTTGAA
ENST00000683500.2:c.14895-201_14895-200insGTTGAA MANE Select ENSP00000508292.2:n.14895-201_14895-200insGTTGAA
ENST00000623487.1:n.3040_3041insGTTGAA
ENST00000624552.3:c.14835-201_14835-200insGTTGAA ENSP00000485357.1:n.14835-201_14835-200insGTTGAA
NM_001291815.1:c.14895-201_14895-200insGTTGAA NP_001278744.1:n.14895-201_14895-200insGTTGAA
XM_011518465.1:c.14772-201_14772-200insGTTGAA XP_011516767.1:n.14772-201_14772-200insGTTGAA
XM_011518466.1:c.14763-201_14763-200insGTTGAA XP_011516768.1:n.14763-201_14763-200insGTTGAA
XM_011518467.1:c.14718-201_14718-200insGTTGAA XP_011516769.1:n.14718-201_14718-200insGTTGAA
NM_001291815.2:c.14895-201_14895-200insGTTGAA MANE Select NP_001278744.1:n.14895-201_14895-200insGTTGAA
XM_011518465.2:c.14772-201_14772-200insGTTGAA XP_011516767.1:n.14772-201_14772-200insGTTGAA
XM_011518466.2:c.14763-201_14763-200insGTTGAA XP_011516768.1:n.14763-201_14763-200insGTTGAA
XM_011518467.2:c.14718-201_14718-200insGTTGAA XP_011516769.1:n.14718-201_14718-200insGTTGAA
XM_017014585.1:c.11676-201_11676-200insGTTGAA XP_016870074.1:n.11676-201_11676-200insGTTGAA
XM_017014586.1:c.7473-201_7473-200insGTTGAA XP_016870075.1:n.7473-201_7473-200insGTTGAA
XR_001746957.1:n.92+473_92+474insTTCAAC
XR_001746958.1:n.92+473_92+474insTTCAAC