Canonical Allele Identifier: CA9091511

Gene: CREB3L3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4170228G>T , CM000681.2:g.4170228G>T	GRCh38
NC_000019.9:g.4170225G>T , CM000681.1:g.4170225G>T	GRCh37
NC_000019.8:g.4121225G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032607.3:c.890+20G>T MANE Select	NP_115996.1:n.890+20G>T
ENST00000078445.7:c.890+20G>T MANE Select	ENSP00000078445.1:n.890+20G>T
NM_001271995.1:c.887+20G>T	NP_001258924.1:n.887+20G>T
NM_001271995.2:c.887+20G>T	NP_001258924.1:n.887+20G>T
NM_001271996.1:c.884+20G>T	NP_001258925.1:n.884+20G>T
NM_001271996.2:c.884+20G>T	NP_001258925.1:n.884+20G>T
NM_001271997.1:c.783+20G>T	NP_001258926.1:n.783+20G>T
NM_001271997.2:c.783+20G>T	NP_001258926.1:n.783+20G>T
NM_032607.2:c.890+20G>T	NP_115996.1:n.890+20G>T
ENST00000078445.6:c.890+20G>T	ENSP00000078445.1:n.890+20G>T
ENST00000595923.5:c.887+20G>T	ENSP00000469355.1:n.887+20G>T
ENST00000598894.1:n.374+20G>T
ENST00000602147.1:c.783+20G>T	ENSP00000470119.1:n.783+20G>T
ENST00000602257.5:c.884+20G>T	ENSP00000472399.1:n.884+20G>T