Canonical Allele Identifier: CA2576091142

Gene: MVD

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88655141_88655142del , CM000678.2:g.88655141_88655142del	GRCh38
NC_000016.9:g.88721549_88721550del , CM000678.1:g.88721549_88721550del	GRCh37
NC_000016.8:g.87249050_87249051del	NCBI36
NG_007291.1:g.910_911del , LRG_52:g.910_911del
NG_052674.1:g.13014_13015del

Transcript Alleles

HGVS	Amino-acid change
ENST00000301012.8:c.897+59_897+60del MANE Select	ENSP00000301012.3:n.897+59_897+60del
ENST00000301012.7:c.897+59_897+60del	ENSP00000301012.3:n.897+59_897+60del
ENST00000565149.5:n.1456+59_1456+60del
ENST00000620002.4:c.380+59_380+60del	ENSP00000479264.1:n.380+59_380+60del
NM_002461.2:c.897+59_897+60del	NP_002452.1:n.897+59_897+60del
XM_011523086.1:c.999+59_999+60del	XP_011521388.1:n.999+59_999+60del
XM_011523087.1:c.936+59_936+60del	XP_011521389.1:n.936+59_936+60del
XM_011523088.1:c.834+59_834+60del	XP_011521390.1:n.834+59_834+60del
XM_011523089.1:c.546+59_546+60del	XP_011521391.1:n.546+59_546+60del
XM_011523086.2:c.999+59_999+60del	XP_011521388.1:n.999+59_999+60del
XM_011523087.2:c.936+59_936+60del	XP_011521389.1:n.936+59_936+60del
XM_011523088.2:c.834+59_834+60del	XP_011521390.1:n.834+59_834+60del
XM_011523089.2:c.546+59_546+60del	XP_011521391.1:n.546+59_546+60del
NM_002461.3:c.897+59_897+60del MANE Select	NP_002452.1:n.897+59_897+60del