Canonical Allele Identifier: CA1619342247

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861247T= , CM000668.2:g.31861247T=	GRCh38
NC_000006.11:g.31829024T= , CM000668.1:g.31829024T=	GRCh37
NC_000006.10:g.31937003T=	NCBI36
NG_008201.1:g.6686A=
NG_023058.1:g.22800A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.556A= MANE Select	ENSP00000364782.4:p.Asn186=
ENST00000677054.1:n.1233A=
ENST00000677512.1:n.664A=
ENST00000678869.1:n.664A=
ENST00000375631.4:c.556A=	ENSP00000364782.4:p.Asn186=
ENST00000480384.1:n.585A=
ENST00000491768.5:c.556A=	ENSP00000433127.1:p.Asn186=
ENST00000495807.1:n.1124A=
NM_000434.3:c.556A=	NP_000425.1:p.Asn186=
NM_000434.4:c.556A= MANE Select	NP_000425.1:p.Asn186=