Canonical Allele Identifier: CA2838472915
Gene: MAN2C1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.75364691G>T , CM000677.2:g.75364691G>T GRCh38
NC_000015.9:g.75657032G>T , CM000677.1:g.75657032G>T GRCh37
NC_000015.8:g.73444085G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000267978.10:c.423-26C>A MANE Select ENSP00000267978.4:n.423-26C>A
ENST00000267978.9:c.423-26C>A ENSP00000267978.4:n.423-26C>A
ENST00000421803.6:c.423-26C>A ENSP00000390738.2:n.423-26C>A
ENST00000561615.1:c.471-26C>A ENSP00000457833.1:n.471-26C>A
ENST00000562071.5:c.*164-26C>A ENSP00000455803.1:n.*164-26C>A
ENST00000563441.5:n.319-26C>A
ENST00000563539.5:n.445-26C>A
ENST00000563622.5:c.423-26C>A ENSP00000454589.1:n.423-26C>A
ENST00000565534.5:n.776-26C>A
ENST00000565683.5:c.423-26C>A ENSP00000457788.1:n.423-26C>A
ENST00000565784.5:c.228-557C>A ENSP00000456419.1:n.228-557C>A
ENST00000566256.5:c.384-26C>A ENSP00000455788.1:n.384-26C>A
ENST00000566634.5:c.228-557C>A ENSP00000456914.1:n.228-557C>A
ENST00000568374.5:c.297-26C>A ENSP00000456257.1:n.297-26C>A
ENST00000569355.5:c.521-26C>A ENSP00000454406.1:n.521-26C>A
ENST00000569482.5:c.423-26C>A ENSP00000455998.1:n.423-26C>A
ENST00000570257.6:c.72-26C>A ENSP00000456667.2:n.72-26C>A
NM_001256494.1:c.423-26C>A NP_001243423.1:n.423-26C>A
NM_001256495.1:c.423-26C>A NP_001243424.1:n.423-26C>A
NM_001256496.1:c.423-26C>A NP_001243425.1:n.423-26C>A
NM_006715.3:c.423-26C>A NP_006706.2:n.423-26C>A
XM_005254384.1:c.423-26C>A XP_005254441.1:n.423-26C>A
XM_011521567.1:c.423-26C>A XP_011519869.1:n.423-26C>A
XM_011521568.1:c.423-26C>A XP_011519870.1:n.423-26C>A
XM_011521569.1:c.-58-26C>A XP_011519871.1:n.-58-26C>A
XR_931832.1:n.954-26C>A
XR_931833.1:n.954-26C>A
XR_931834.1:n.954-26C>A
XR_931835.1:n.954-26C>A
XM_005254384.3:c.423-26C>A XP_005254441.1:n.423-26C>A
XM_017022186.1:c.468-26C>A XP_016877675.1:n.468-26C>A
XM_017022187.1:c.468-26C>A XP_016877676.1:n.468-26C>A
XM_017022188.2:c.423-26C>A XP_016877677.1:n.423-26C>A
XR_001751282.1:n.815-26C>A
XR_001751283.1:n.815-26C>A
XR_001751284.1:n.815-26C>A
XR_001751285.1:n.815-26C>A
XR_001751286.1:n.815-26C>A
XR_001751287.1:n.815-26C>A
XR_001751288.1:n.815-26C>A
XR_002957638.1:n.815-26C>A
XR_002957639.1:n.439-26C>A
NM_006715.4:c.423-26C>A MANE Select NP_006706.2:n.423-26C>A
NM_001256494.2:c.423-26C>A NP_001243423.1:n.423-26C>A
NM_001256495.2:c.423-26C>A NP_001243424.1:n.423-26C>A
NM_001256496.2:c.423-26C>A NP_001243425.1:n.423-26C>A