Canonical Allele Identifier: CA9091492

Gene: CREB3L3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4170124G>A , CM000681.2:g.4170124G>A	GRCh38
NC_000019.9:g.4170121G>A , CM000681.1:g.4170121G>A	GRCh37
NC_000019.8:g.4121121G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032607.3:c.822-16G>A MANE Select	NP_115996.1:n.822-16G>A
ENST00000078445.7:c.822-16G>A MANE Select	ENSP00000078445.1:n.822-16G>A
NM_001271995.1:c.819-16G>A	NP_001258924.1:n.819-16G>A
NM_001271995.2:c.819-16G>A	NP_001258924.1:n.819-16G>A
NM_001271996.1:c.816-16G>A	NP_001258925.1:n.816-16G>A
NM_001271996.2:c.816-16G>A	NP_001258925.1:n.816-16G>A
NM_001271997.1:c.715-16G>A	NP_001258926.1:n.715-16G>A
NM_001271997.2:c.715-16G>A	NP_001258926.1:n.715-16G>A
NM_032607.2:c.822-16G>A	NP_115996.1:n.822-16G>A
ENST00000078445.6:c.822-16G>A	ENSP00000078445.1:n.822-16G>A
ENST00000595923.5:c.819-16G>A	ENSP00000469355.1:n.819-16G>A
ENST00000598894.1:n.306-16G>A
ENST00000602147.1:c.715-16G>A	ENSP00000470119.1:n.715-16G>A
ENST00000602257.5:c.816-16G>A	ENSP00000472399.1:n.816-16G>A