Canonical Allele Identifier: CA1619342382

Gene: NEU1

Linked Data

• dbSNP Id: rs1762516678

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861590_31861591del , CM000668.2:g.31861590_31861591del	GRCh38
NC_000006.11:g.31829367_31829368del , CM000668.1:g.31829367_31829368del	GRCh37
NC_000006.10:g.31937346_31937347del	NCBI36
NG_008201.1:g.6343_6344del
NG_023058.1:g.22457_22458del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-140_353-139del MANE Select	ENSP00000364782.4:n.353-140_353-139del
ENST00000677054.1:n.890_891del
ENST00000677512.1:n.461-140_461-139del
ENST00000678869.1:n.461-140_461-139del
ENST00000375631.4:c.353-140_353-139del	ENSP00000364782.4:n.353-140_353-139del
ENST00000480384.1:n.382-140_382-139del
ENST00000491768.5:c.353-140_353-139del	ENSP00000433127.1:n.353-140_353-139del
ENST00000495807.1:n.781_782del
NM_000434.3:c.353-140_353-139del	NP_000425.1:n.353-140_353-139del
NM_000434.4:c.353-140_353-139del MANE Select	NP_000425.1:n.353-140_353-139del