Canonical Allele Identifier: CA363486663

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31827825C>A (hg19) ; chr6:g.31860048C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31860048C>A , CM000668.2:g.31860048C>A	GRCh38
NC_000006.11:g.31827825C>A , CM000668.1:g.31827825C>A	GRCh37
NC_000006.10:g.31935804C>A	NCBI36
NG_008201.1:g.7885G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.1015G>T MANE Select	ENSP00000364782.4:p.Glu339Ter
ENST00000677054.1:n.2258G>T
ENST00000677512.1:n.1297G>T
ENST00000678869.1:n.1603G>T
ENST00000375631.4:c.1015G>T	ENSP00000364782.4:p.Glu339Ter
ENST00000480384.1:n.1218G>T
ENST00000491768.5:c.*125G>T	ENSP00000433127.1:n.*125G>T
ENST00000495807.1:n.2323G>T
NM_000434.3:c.1015G>T	NP_000425.1:p.Glu339Ter
NM_000434.4:c.1015G>T MANE Select	NP_000425.1:p.Glu339Ter