Canonical Allele Identifier: CA2663623987
Gene: CHRND HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232534369_232534370insTGTTCAAGT , CM000664.2:g.232534369_232534370insTGTTCAAGT GRCh38
NC_000002.11:g.233399079_233399080insTGTTCAAGT , CM000664.1:g.233399079_233399080insTGTTCAAGT GRCh37
NC_000002.10:g.233107323_233107324insTGTTCAAGT NCBI36
NG_008028.1:g.13158_13159insTGTTCAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000258385.8:c.1371+27_1371+28insTGTTCAAGT MANE Select ENSP00000258385.3:n.1371+27_1371+28insTGTTCAAGT
ENST00000258385.7:c.1371+27_1371+28insTGTTCAAGT ENSP00000258385.3:n.1371+27_1371+28insTGTTCAAGT
ENST00000441621.6:c.*553+27_*553+28insTGTTCAAGT ENSP00000408819.2:n.*553+27_*553+28insTGTTCAAGT
ENST00000446616.1:c.*1012+27_*1012+28insTGTTCAAGT ENSP00000410801.1:n.*1012+27_*1012+28insTGTTCAAGT
ENST00000543200.5:c.1326+27_1326+28insTGTTCAAGT ENSP00000438380.1:n.1326+27_1326+28insTGTTCAAGT
NM_000751.2:c.1371+27_1371+28insTGTTCAAGT NP_000742.1:n.1371+27_1371+28insTGTTCAAGT
NM_001256657.1:c.1326+27_1326+28insTGTTCAAGT NP_001243586.1:n.1326+27_1326+28insTGTTCAAGT
NM_001311195.1:c.789+27_789+28insTGTTCAAGT NP_001298124.1:n.789+27_789+28insTGTTCAAGT
NM_001311196.1:c.1068+27_1068+28insTGTTCAAGT NP_001298125.1:n.1068+27_1068+28insTGTTCAAGT
NR_046333.1:c.-4294966180+27_-4294966180+28insTGTTCAAGT
NR_046334.1:c.-4294965901+27_-4294965901+28insTGTTCAAGT
XM_011510524.1:c.990+27_990+28insTGTTCAAGT XP_011508826.1:n.990+27_990+28insTGTTCAAGT
XM_011510524.2:c.990+27_990+28insTGTTCAAGT XP_011508826.1:n.990+27_990+28insTGTTCAAGT
NM_000751.3:c.1371+27_1371+28insTGTTCAAGT MANE Select NP_000742.1:n.1371+27_1371+28insTGTTCAAGT
NM_001311195.2:c.789+27_789+28insTGTTCAAGT NP_001298124.1:n.789+27_789+28insTGTTCAAGT
NM_001311196.2:c.1068+27_1068+28insTGTTCAAGT NP_001298125.1:n.1068+27_1068+28insTGTTCAAGT
NM_001256657.2:c.1326+27_1326+28insTGTTCAAGT NP_001243586.1:n.1326+27_1326+28insTGTTCAAGT