Canonical Allele Identifier: CA1881266049

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433291_130433294delinsGCCA , CM000671.2:g.130433291_130433294delinsGCCA	GRCh38
NC_000009.11:g.133308678_133308681delinsGCCA , CM000671.1:g.133308678_133308681delinsGCCA	GRCh37
NC_000009.10:g.132298499_132298502delinsGCCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-57_14838-54delinsGCCA	ENSP00000485357.2:n.14838-57_14838-54delinsGCCA
ENST00000683500.2:c.14895-57_14895-54delinsGCCA MANE Select	ENSP00000508292.2:n.14895-57_14895-54delinsGCCA
ENST00000623487.1:n.3184_3187delinsGCCA
ENST00000624552.3:c.14835-57_14835-54delinsGCCA	ENSP00000485357.1:n.14835-57_14835-54delinsGCCA
NM_001291815.1:c.14895-57_14895-54delinsGCCA	NP_001278744.1:n.14895-57_14895-54delinsGCCA
XM_011518465.1:c.14772-57_14772-54delinsGCCA	XP_011516767.1:n.14772-57_14772-54delinsGCCA
XM_011518466.1:c.14763-57_14763-54delinsGCCA	XP_011516768.1:n.14763-57_14763-54delinsGCCA
XM_011518467.1:c.14718-57_14718-54delinsGCCA	XP_011516769.1:n.14718-57_14718-54delinsGCCA
NM_001291815.2:c.14895-57_14895-54delinsGCCA MANE Select	NP_001278744.1:n.14895-57_14895-54delinsGCCA
XM_011518465.2:c.14772-57_14772-54delinsGCCA	XP_011516767.1:n.14772-57_14772-54delinsGCCA
XM_011518466.2:c.14763-57_14763-54delinsGCCA	XP_011516768.1:n.14763-57_14763-54delinsGCCA
XM_011518467.2:c.14718-57_14718-54delinsGCCA	XP_011516769.1:n.14718-57_14718-54delinsGCCA
XM_017014585.1:c.11676-57_11676-54delinsGCCA	XP_016870074.1:n.11676-57_11676-54delinsGCCA
XM_017014586.1:c.7473-57_7473-54delinsGCCA	XP_016870075.1:n.7473-57_7473-54delinsGCCA
XR_001746957.1:n.92+327_92+330delinsTGGC
XR_001746958.1:n.92+327_92+330delinsTGGC