Canonical Allele Identifier: CA1619341618

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859729C= , CM000668.2:g.31859729C=	GRCh38
NC_000006.11:g.31827506C= , CM000668.1:g.31827506C=	GRCh37
NC_000006.10:g.31935485C=	NCBI36
NG_008201.1:g.8204G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.1238G= MANE Select	ENSP00000364782.4:p.Gly413=
ENST00000677054.1:n.2577G=
ENST00000677512.1:n.1515G=
ENST00000678869.1:n.1826G=
ENST00000375631.4:c.1238G=	ENSP00000364782.4:p.Gly413=
ENST00000480384.1:n.1537G=
ENST00000491768.5:c.*348G=	ENSP00000433127.1:n.*348G=
ENST00000495807.1:n.2546G=
NM_000434.3:c.1238G=	NP_000425.1:p.Gly413=
NM_000434.4:c.1238G= MANE Select	NP_000425.1:p.Gly413=