Canonical Allele Identifier: CA16118467

Gene: CERS6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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