Canonical Allele Identifier: CA415844222

Gene: RERE

Linked Data

• gnomAD v4: 1-8359776-T-G
• MyVariant Identifiers: chr1:g.8419836T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8359776T>G , CM000663.2:g.8359776T>G	GRCh38
NC_000001.10:g.8419836T>G , CM000663.1:g.8419836T>G	GRCh37
NC_000001.9:g.8342423T>G	NCBI36
NG_047035.1:g.462916A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1944A>C	ENSP00000515651.1:p.Ala648=
ENST00000400908.7:c.3606A>C MANE Select	ENSP00000383700.2:p.Ala1202=
ENST00000337907.7:c.3606A>C	ENSP00000338629.3:p.Ala1202=
ENST00000377464.5:c.2802A>C	ENSP00000366684.1:p.Ala934=
ENST00000400907.6:c.1541-4177A>C	ENSP00000383699.2:n.1541-4177A>C
ENST00000400908.6:c.3606A>C	ENSP00000383700.2:p.Ala1202=
ENST00000476556.5:c.1944A>C	ENSP00000422246.1:p.Ala648=
ENST00000505225.1:c.307+1684A>C	ENSP00000423451.1:n.307+1684A>C
NM_001042681.1:c.3606A>C	NP_001036146.1:p.Ala1202=
NM_001042682.1:c.1944A>C	NP_001036147.1:p.Ala648=
NM_012102.3:c.3606A>C	NP_036234.3:p.Ala1202=
XM_005263464.1:c.3606A>C	XP_005263521.1:p.Ala1202=
XM_005263466.1:c.2802A>C	XP_005263523.1:p.Ala934=
XM_006710653.1:c.3606A>C	XP_006710716.1:p.Ala1202=
XM_011541510.1:c.3480A>C	XP_011539812.1:p.Ala1160=
XM_011541511.1:c.3395+336A>C	XP_011539813.1:n.3395+336A>C
XM_005263464.2:c.3606A>C	XP_005263521.1:p.Ala1202=
XM_011541510.2:c.3480A>C	XP_011539812.1:p.Ala1160=
XM_011541511.2:c.3395+336A>C	XP_011539813.1:n.3395+336A>C
XM_017001358.1:c.3606A>C	XP_016856847.1:p.Ala1202=
XM_017001359.1:c.3606A>C	XP_016856848.1:p.Ala1202=
NM_001042681.2:c.3606A>C MANE Select	NP_001036146.1:p.Ala1202=
NM_001042682.2:c.1944A>C	NP_001036147.1:p.Ala648=
NM_012102.4:c.3606A>C	NP_036234.3:p.Ala1202=