Canonical Allele Identifier: CA1619342348

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861497_31861512delinsACCCTTTCTACCACTT , CM000668.2:g.31861497_31861512delinsACCCTTTCTACCACTT	GRCh38
NC_000006.11:g.31829274_31829289delinsACCCTTTCTACCACTT , CM000668.1:g.31829274_31829289delinsACCCTTTCTACCACTT	GRCh37
NC_000006.10:g.31937253_31937268delinsACCCTTTCTACCACTT	NCBI36
NG_008201.1:g.6421_6436delinsAAGTGGTAGAAAGGGT
NG_023058.1:g.22535_22550delinsAAGTGGTAGAAAGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-62_353-47delinsAAGTGGTAGAAAGGGT MANE Select	ENSP00000364782.4:n.353-62_353-47delinsAAGTGGTAGAAAGGGT
ENST00000677054.1:n.968_983delinsAAGTGGTAGAAAGGGT
ENST00000677512.1:n.461-62_461-47delinsAAGTGGTAGAAAGGGT
ENST00000678869.1:n.461-62_461-47delinsAAGTGGTAGAAAGGGT
ENST00000375631.4:c.353-62_353-47delinsAAGTGGTAGAAAGGGT	ENSP00000364782.4:n.353-62_353-47delinsAAGTGGTAGAAAGGGT
ENST00000480384.1:n.382-62_382-47delinsAAGTGGTAGAAAGGGT
ENST00000491768.5:c.353-62_353-47delinsAAGTGGTAGAAAGGGT	ENSP00000433127.1:n.353-62_353-47delinsAAGTGGTAGAAAGGGT
ENST00000495807.1:n.859_874delinsAAGTGGTAGAAAGGGT
NM_000434.3:c.353-62_353-47delinsAAGTGGTAGAAAGGGT	NP_000425.1:n.353-62_353-47delinsAAGTGGTAGAAAGGGT
NM_000434.4:c.353-62_353-47delinsAAGTGGTAGAAAGGGT MANE Select	NP_000425.1:n.353-62_353-47delinsAAGTGGTAGAAAGGGT