Canonical Allele Identifier: CA338170608

Gene: RERE

Linked Data

• gnomAD v4: 1-8359958-T-C
• MyVariant Identifiers: chr1:g.8420018T>C (hg19) ; chr1:g.8359958T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8359958T>C , CM000663.2:g.8359958T>C	GRCh38
NC_000001.10:g.8420018T>C , CM000663.1:g.8420018T>C	GRCh37
NC_000001.9:g.8342605T>C	NCBI36
NG_047035.1:g.462734A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1762A>G	ENSP00000515651.1:p.Asn588Asp
ENST00000400908.7:c.3424A>G MANE Select	ENSP00000383700.2:p.Asn1142Asp
ENST00000337907.7:c.3424A>G	ENSP00000338629.3:p.Asn1142Asp
ENST00000377464.5:c.2620A>G	ENSP00000366684.1:p.Asn874Asp
ENST00000400907.6:c.1541-4359A>G	ENSP00000383699.2:n.1541-4359A>G
ENST00000400908.6:c.3424A>G	ENSP00000383700.2:p.Asn1142Asp
ENST00000476556.5:c.1762A>G	ENSP00000422246.1:p.Asn588Asp
ENST00000505225.1:c.307+1502A>G	ENSP00000423451.1:n.307+1502A>G
NM_001042681.1:c.3424A>G	NP_001036146.1:p.Asn1142Asp
NM_001042682.1:c.1762A>G	NP_001036147.1:p.Asn588Asp
NM_012102.3:c.3424A>G	NP_036234.3:p.Asn1142Asp
XM_005263464.1:c.3424A>G	XP_005263521.1:p.Asn1142Asp
XM_005263466.1:c.2620A>G	XP_005263523.1:p.Asn874Asp
XM_006710653.1:c.3424A>G	XP_006710716.1:p.Asn1142Asp
XM_011541510.1:c.3298A>G	XP_011539812.1:p.Asn1100Asp
XM_011541511.1:c.3395+154A>G	XP_011539813.1:n.3395+154A>G
XM_005263464.2:c.3424A>G	XP_005263521.1:p.Asn1142Asp
XM_011541510.2:c.3298A>G	XP_011539812.1:p.Asn1100Asp
XM_011541511.2:c.3395+154A>G	XP_011539813.1:n.3395+154A>G
XM_017001358.1:c.3424A>G	XP_016856847.1:p.Asn1142Asp
XM_017001359.1:c.3424A>G	XP_016856848.1:p.Asn1142Asp
NM_001042681.2:c.3424A>G MANE Select	NP_001036146.1:p.Asn1142Asp
NM_001042682.2:c.1762A>G	NP_001036147.1:p.Asn588Asp
NM_012102.4:c.3424A>G	NP_036234.3:p.Asn1142Asp