Canonical Allele Identifier: CA1910256985
Gene: MBL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52766221_52766222delinsGA , CM000672.2:g.52766221_52766222delinsGA GRCh38
NC_000010.10:g.54525981_54525982delinsGA , CM000672.1:g.54525981_54525982delinsGA GRCh37
NC_000010.9:g.54195987_54195988delinsGA NCBI36
NG_008196.1:g.10479_10480delinsTC , LRG_154:g.10479_10480delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000674931.1:c.*1915_*1916delinsTC MANE Select ENSP00000502789.1:n.*1915_*1916delinsTC
ENST00000675947.1:c.*1915_*1916delinsTC ENSP00000502615.1:n.*1915_*1916delinsTC
ENST00000373968.3:c.*1915_*1916delinsTC ENSP00000363079.3:n.*1915_*1916delinsTC
NM_000242.2:c.*1915_*1916delinsTC , LRG_154t1:c.*1915_*1916delinsTC NP_000233.1:n.*1915_*1916delinsTC
XM_006717861.2:c.*1915_*1916delinsTC XP_006717924.1:n.*1915_*1916delinsTC
XM_011539816.1:c.*1915_*1916delinsTC XP_011538118.1:n.*1915_*1916delinsTC
XM_006717861.4:c.*1915_*1916delinsTC XP_006717924.1:n.*1915_*1916delinsTC
XM_011539816.3:c.*1915_*1916delinsTC XP_011538118.1:n.*1915_*1916delinsTC
NM_000242.3:c.*1915_*1916delinsTC NP_000233.1:n.*1915_*1916delinsTC
NM_001378373.1:c.*1915_*1916delinsTC MANE Select NP_001365302.1:n.*1915_*1916delinsTC
NM_001378374.1:c.*1915_*1916delinsTC NP_001365303.1:n.*1915_*1916delinsTC