Canonical Allele Identifier: CA1619341748

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31860036_31860038delinsACT , CM000668.2:g.31860036_31860038delinsACT	GRCh38
NC_000006.11:g.31827813_31827815delinsACT , CM000668.1:g.31827813_31827815delinsACT	GRCh37
NC_000006.10:g.31935792_31935794delinsACT	NCBI36
NG_008201.1:g.7895_7897delinsAGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.1021+4_1021+6delinsAGT MANE Select	ENSP00000364782.4:n.1021+4_1021+6delinsAG...
ENST00000677054.1:n.2268_2270delinsAGT
ENST00000677512.1:n.1298+9_1298+11delinsAGT
ENST00000678869.1:n.1609+4_1609+6delinsAGT
ENST00000375631.4:c.1021+4_1021+6delinsAGT	ENSP00000364782.4:n.1021+4_1021+6delinsAG...
ENST00000480384.1:n.1228_1230delinsAGT
ENST00000491768.5:c.*131+4_*131+6delinsAGT	ENSP00000433127.1:n.*131+4_*131+6delinsAG...
ENST00000495807.1:n.2329+4_2329+6delinsAGT
NM_000434.3:c.1021+4_1021+6delinsAGT	NP_000425.1:n.1021+4_1021+6delinsAGT
NM_000434.4:c.1021+4_1021+6delinsAGT MANE Select	NP_000425.1:n.1021+4_1021+6delinsAGT