Canonical Allele Identifier: CA2830537847

Gene: MND1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153350305_153350306insAC , CM000666.2:g.153350305_153350306insAC	GRCh38
NC_000004.11:g.154271457_154271458insAC , CM000666.1:g.154271457_154271458insAC	GRCh37
NC_000004.10:g.154490907_154490908insAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000240488.8:c.69+176_69+177insAC MANE Select	ENSP00000240488.3:n.69+176_69+177insAC
ENST00000674680.1:c.*1613+176_*1613+177insAC	ENSP00000502469.1:n.*1613+176_*1613+177insAC
ENST00000674967.1:c.2148+176_2148+177insAC	ENSP00000501627.1:n.2148+176_2148+177insAC
ENST00000675079.1:c.2160+176_2160+177insAC	ENSP00000502677.1:n.2160+176_2160+177insAC
ENST00000675518.1:c.1815+176_1815+177insAC	ENSP00000501852.1:n.1815+176_1815+177insAC
ENST00000675838.1:c.2148+176_2148+177insAC	ENSP00000501593.1:n.2148+176_2148+177insAC
ENST00000240488.7:c.69+176_69+177insAC	ENSP00000240488.3:n.69+176_69+177insAC
ENST00000503967.1:n.145+176_145+177insAC
ENST00000504860.2:c.24+176_24+177insAC	ENSP00000422933.1:n.24+176_24+177insAC
ENST00000508731.5:c.24+176_24+177insAC	ENSP00000425500.1:n.24+176_24+177insAC
ENST00000509752.5:c.69+176_69+177insAC	ENSP00000427559.1:n.69+176_69+177insAC
ENST00000622785.4:c.69+176_69+177insAC	ENSP00000477758.1:n.69+176_69+177insAC
NM_001253861.1:c.69+176_69+177insAC	NP_001240790.1:n.69+176_69+177insAC
NM_032117.3:c.69+176_69+177insAC	NP_115493.1:n.69+176_69+177insAC
NR_045605.1:n.158+176_158+177insAC
XM_005263275.1:c.69+176_69+177insAC	XP_005263332.1:n.69+176_69+177insAC
XM_005263275.2:c.69+176_69+177insAC	XP_005263332.1:n.69+176_69+177insAC
XM_017008688.2:c.24+176_24+177insAC	XP_016864177.1:n.24+176_24+177insAC
XM_024454242.1:c.24+176_24+177insAC	XP_024310010.1:n.24+176_24+177insAC
NM_032117.4:c.69+176_69+177insAC MANE Select	NP_115493.1:n.69+176_69+177insAC
NR_045605.2:n.119+176_119+177insAC