Canonical Allele Identifier: CA364105964
Gene: GUCA1ANB-GUCA1A HGNC NCBI
GUCA1A HGNC NCBI
CIMIP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42173768C>A , CM000668.2:g.42173768C>A GRCh38
NC_000006.11:g.42141506C>A , CM000668.1:g.42141506C>A GRCh37
NC_000006.10:g.42249484C>A NCBI36
NG_009938.1:g.23363C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703265.1:c.*390C>A (GUCA1ANB-GUCA1A) ENSP00000515250.1:n.*390C>A
ENST00000703266.1:c.*390C>A (GUCA1ANB-GUCA1A) ENSP00000515251.1:n.*390C>A
ENST00000703267.1:c.*653C>A (GUCA1ANB-GUCA1A) ENSP00000515252.1:n.*653C>A
ENST00000372958.2:c.155C>A (GUCA1A) MANE Select ENSP00000362049.1:p.Ala52Asp
ENST00000394237.6:c.*653C>A (CIMIP3) ENSP00000377784.2:n.*653C>A
ENST00000418175.6:c.*390C>A (CIMIP3) ENSP00000388438.2:n.*390C>A
ENST00000654459.1:c.155C>A (GUCA1A) ENSP00000499539.1:p.Ala52Asp
ENST00000659095.1:c.*390C>A (CIMIP3) ENSP00000499714.1:n.*390C>A
ENST00000053469.8:c.155C>A (GUCA1A) ENSP00000053469.4:p.Ala52Asp
ENST00000372958.1:c.155C>A (GUCA1A) ENSP00000362049.1:p.Ala52Asp
ENST00000394237.5:c.155C>A (GUCA1A) ENSP00000377784.1:p.Ala52Asp
ENST00000418175.5:c.155C>A (GUCA1A) ENSP00000388438.1:p.Ala52Asp
ENST00000541991.5:c.143C>A (GUCA1A) ENSP00000437476.2:p.Ala48Asp
NM_000409.3:c.155C>A (GUCA1A) NP_000400.2:p.Ala52Asp
XM_006715073.2:c.-128C>A (GUCA1A) XP_006715136.1:n.-128C>A
XM_011514536.1:c.155C>A (GUCA1A) XP_011512838.1:p.Ala52Asp
XM_011514537.1:c.155C>A (GUCA1A) XP_011512839.1:p.Ala52Asp
XM_011514538.1:c.155C>A (GUCA1A) XP_011512840.1:p.Ala52Asp
XM_011514539.1:c.155C>A (GUCA1A) XP_011512841.1:p.Ala52Asp
NM_000409.4:c.155C>A (GUCA1A) NP_000400.2:p.Ala52Asp
NM_001319061.1:c.155C>A (GUCA1A) NP_001305990.1:p.Ala52Asp
NM_001319062.1:c.155C>A (GUCA1A) NP_001305991.1:p.Ala52Asp
XM_011514537.2:c.155C>A (GUCA1A) XP_011512839.1:p.Ala52Asp
NM_000409.5:c.155C>A (GUCA1A) NP_000400.2:p.Ala52Asp
NM_001319061.2:c.155C>A (GUCA1A) NP_001305990.1:p.Ala52Asp
NM_001319062.2:c.155C>A (GUCA1A) NP_001305991.1:p.Ala52Asp
NM_001384910.1:c.155C>A (GUCA1A) MANE Select NP_001371839.1:p.Ala52Asp