Canonical Allele Identifier: CA1619341957

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31860511G= , CM000668.2:g.31860511G=	GRCh38
NC_000006.11:g.31828288G= , CM000668.1:g.31828288G=	GRCh37
NC_000006.10:g.31936267G=	NCBI36
NG_008201.1:g.7422C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.726C= MANE Select	ENSP00000364782.4:p.Tyr242=
ENST00000677054.1:n.1969C=
ENST00000677512.1:n.834C=
ENST00000678869.1:n.1400C=
ENST00000375631.4:c.726C=	ENSP00000364782.4:p.Tyr242=
ENST00000480384.1:n.755C=
ENST00000491768.5:c.726C=	ENSP00000433127.1:p.Tyr242=
ENST00000495807.1:n.1860C=
NM_000434.3:c.726C=	NP_000425.1:p.Tyr242=
NM_000434.4:c.726C= MANE Select	NP_000425.1:p.Tyr242=