Canonical Allele Identifier: CA1306026285
Gene: CERS6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168532581G= , CM000664.2:g.168532581G= GRCh38
NC_000002.11:g.169389091G= , CM000664.1:g.169389091G= GRCh37
NC_000002.10:g.169097337G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305747.11:c.171-15015G= MANE Select ENSP00000306579.6:n.171-15015G=
ENST00000305747.10:c.171-15015G= ENSP00000306579.6:n.171-15015G=
ENST00000392687.4:c.171-15015G= ENSP00000376453.4:n.171-15015G=
NM_001256126.1:c.171-15015G= NP_001243055.1:n.171-15015G=
NM_203463.2:c.171-15015G= NP_982288.1:n.171-15015G=
XM_024452780.1:c.171-15015G= XP_024308548.1:n.171-15015G=
XM_024452781.1:c.171-15015G= XP_024308549.1:n.171-15015G=
NM_001256126.2:c.171-15015G= NP_001243055.1:n.171-15015G=
NM_203463.3:c.171-15015G= MANE Select NP_982288.1:n.171-15015G=