Canonical Allele Identifier: CA2669843636
Gene: WFS1 HGNC NCBI

Linked Data

gnomAD v4: 4-6302621-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302621A>C , CM000666.2:g.6302621A>C GRCh38
NC_000004.11:g.6304348A>C , CM000666.1:g.6304348A>C GRCh37
NC_000004.10:g.6355249A>C NCBI36
NG_011700.1:g.37772A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.*153A>C ENSP00000507852.1:n.*153A>C
ENST00000683395.1:c.2803A>C
ENST00000684087.1:c.*153A>C ENSP00000506978.1:n.*153A>C
ENST00000506362.2:c.*153A>C ENSP00000424103.2:n.*153A>C
ENST00000673991.1:c.*153A>C ENSP00000501033.1:n.*153A>C
ENST00000226760.5:c.*153A>C MANE Select ENSP00000226760.1:n.*153A>C
ENST00000503569.5:c.*153A>C ENSP00000423337.1:n.*153A>C
ENST00000507765.1:n.3011A>C
NM_001145853.1:c.*153A>C NP_001139325.1:n.*153A>C
NM_006005.3:c.*153A>C MANE Select NP_005996.2:n.*153A>C
XM_017008586.1:c.*153A>C XP_016864075.1:n.*153A>C
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