Canonical Allele Identifier: CA2323503500
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12657058_12657083delinsTGCGGAAGAGCGCAAAGGGACCGGTG , CM000681.2:g.12657058_12657083delinsTGCGGAAGAGCGCAAAGGGACCGGTG GRCh38
NC_000019.9:g.12767872_12767897delinsTGCGGAAGAGCGCAAAGGGACCGGTG , CM000681.1:g.12767872_12767897delinsTGCGGAAGAGCGCAAAGGGACCGGTG GRCh37
NC_000019.8:g.12628872_12628897delinsTGCGGAAGAGCGCAAAGGGACCGGTG NCBI36
NG_008318.1:g.14695_14720delinsCACCGGTCCCTTTGCGCTCTTCCGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000456935.7:c.1420-27_1420-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA MANE Select ENSP00000395473.2:n.1420-27_1420-2delinsCACCGGTCCCTTTGCGCTCTT...
ENST00000221363.8:c.1417-27_1417-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA ENSP00000221363.4:n.1417-27_1417-2delinsCACCGGTCCCTTTGCGCTCTT...
ENST00000433513.5:n.26-27_26-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA
ENST00000456935.6:c.1420-27_1420-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA ENSP00000395473.2:n.1420-27_1420-2delinsCACCGGTCCCTTTGCGCTCTT...
ENST00000466794.5:n.1319-27_1319-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA
ENST00000495617.1:n.596-27_596-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA
ENST00000593686.1:c.30-27_30-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA
ENST00000595880.5:n.17-27_17-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA
NM_000528.3:c.1420-27_1420-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA NP_000519.2:n.1420-27_1420-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA
NM_001173498.1:c.1417-27_1417-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA NP_001166969.1:n.1417-27_1417-2delinsCACCGGTCCCTTTGCGCTCTTCCG...
XM_005259913.1:c.1423-27_1423-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA XP_005259970.1:n.1423-27_1423-2delinsCACCGGTCCCTTTGCGCTCTTCCG...
XM_011528017.1:c.319-27_319-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA XP_011526319.1:n.319-27_319-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA...
XM_005259913.2:c.1423-27_1423-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA XP_005259970.1:n.1423-27_1423-2delinsCACCGGTCCCTTTGCGCTCTTCCG...
XM_024451518.1:c.319-27_319-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA XP_024307286.1:n.319-27_319-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA...
NM_000528.4:c.1420-27_1420-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA MANE Select NP_000519.2:n.1420-27_1420-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA
NM_001173498.2:c.1417-27_1417-2delinsCACCGGTCCCTTTGCGCTCTTCCGCA NP_001166969.1:n.1417-27_1417-2delinsCACCGGTCCCTTTGCGCTCTTCCG...