Canonical Allele Identifier: CA1039017136

Gene: CERS6

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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