Canonical Allele Identifier: CA376717603

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49471044-G-A
• MyVariant Identifiers: chr10:g.50679090G>A (hg19) ; chr10:g.49471044G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49471044G>A , CM000672.2:g.49471044G>A	GRCh38
NC_000010.10:g.50679090G>A , CM000672.1:g.50679090G>A	GRCh37
NC_000010.9:g.50349096G>A	NCBI36
NG_009442.1:g.73058C>T , LRG_465:g.73058C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3001C>T MANE Select	ENSP00000348089.5:p.Leu1001Phe
ENST00000679552.1:n.142-155C>T
ENST00000679871.1:n.147C>T
ENST00000679974.1:n.120-155C>T
ENST00000681632.1:n.4404C>T
ENST00000681659.1:c.2842C>T	ENSP00000505631.1:p.Leu948Phe
ENST00000355832.9:c.3001C>T	ENSP00000348089.5:p.Leu1001Phe
ENST00000623073.3:c.*1297C>T	ENSP00000485650.1:n.*1297C>T
ENST00000623115.3:c.1111C>T	ENSP00000485321.1:p.Leu371Phe
ENST00000624341.3:c.833C>T
NM_000124.3:c.3001C>T	NP_000115.1:p.Leu1001Phe
XR_945953.1:n.243-521G>A
NM_001346440.1:c.3001C>T	NP_001333369.1:p.Leu1001Phe
NM_000124.4:c.3001C>T MANE Select	NP_000115.1:p.Leu1001Phe
NM_001346440.2:c.3001C>T	NP_001333369.1:p.Leu1001Phe