Canonical Allele Identifier: CA443418975

Gene: RETREG1 RETREG1-AS1

Linked Data

• gnomAD v4: 5-16616960-C-G
• MyVariant Identifiers: chr5:g.16617069C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.16616960C>G , CM000667.2:g.16616960C>G	GRCh38
NC_000005.9:g.16617069C>G , CM000667.1:g.16617069C>G	GRCh37
NC_000005.8:g.16670069C>G	NCBI36
NG_016644.2:g.5050G>C , LRG_363:g.5050G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000509048.2:n.42G>C (RETREG1)
ENST00000682229.1:c.12G>C (RETREG1)	ENSP00000507342.1:p.Pro4=
ENST00000682564.1:c.12G>C (RETREG1)	ENSP00000508099.1:p.Pro4=
ENST00000682808.1:n.79G>C (RETREG1)
ENST00000682828.1:n.9G>C (RETREG1)
ENST00000682982.1:n.35G>C (RETREG1)
ENST00000683045.1:n.38G>C (RETREG1)
ENST00000683527.1:c.12G>C (RETREG1)	ENSP00000507253.1:p.Pro4=
ENST00000683973.1:n.38G>C (RETREG1)
ENST00000684521.1:c.12G>C (RETREG1)	ENSP00000507521.1:p.Pro4=
ENST00000684695.1:n.30G>C (RETREG1)
ENST00000306320.10:c.12G>C (RETREG1) MANE Select	ENSP00000304642.9:p.Pro4=
ENST00000306320.9:c.12G>C (RETREG1)	ENSP00000304642.9:p.Pro4=
ENST00000509048.1:n.79G>C (RETREG1)
NM_001034850.2:c.12G>C , LRG_363t1:c.12G>C (RETREG1)	NP_001030022.1:p.Pro4=
NR_109946.1:n.561+474C>G (RETREG1-AS1)
XM_011514053.1:c.12G>C (RETREG1)	XP_011512355.1:p.Pro4=
XM_011514053.3:c.12G>C (RETREG1)	XP_011512355.1:p.Pro4=
NM_001034850.3:c.12G>C (RETREG1) MANE Select	NP_001030022.1:p.Pro4=