Canonical Allele Identifier: CA2571169817

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861578_31861586del , CM000668.2:g.31861578_31861586del	GRCh38
NC_000006.11:g.31829355_31829363del , CM000668.1:g.31829355_31829363del	GRCh37
NC_000006.10:g.31937334_31937342del	NCBI36
NG_008201.1:g.6347_6355del
NG_023058.1:g.22461_22469del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-136_353-128del MANE Select	ENSP00000364782.4:n.353-136_353-128del
ENST00000677054.1:n.894_902del
ENST00000677512.1:n.461-136_461-128del
ENST00000678869.1:n.461-136_461-128del
ENST00000375631.4:c.353-136_353-128del	ENSP00000364782.4:n.353-136_353-128del
ENST00000480384.1:n.382-136_382-128del
ENST00000491768.5:c.353-136_353-128del	ENSP00000433127.1:n.353-136_353-128del
ENST00000495807.1:n.785_793del
NM_000434.3:c.353-136_353-128del	NP_000425.1:n.353-136_353-128del
NM_000434.4:c.353-136_353-128del MANE Select	NP_000425.1:n.353-136_353-128del