Canonical Allele Identifier: CA120148

Gene: GUCA1ANB-GUCA1A GUCA1A CIMIP3

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42178374A>G , CM000668.2:g.42178374A>G	GRCh38
NC_000006.11:g.42146112A>G , CM000668.1:g.42146112A>G	GRCh37
NC_000006.10:g.42254090A>G	NCBI36
NG_009938.1:g.27969A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703266.1:c.*531A>G (GUCA1ANB-GUCA1A)	ENSP00000515251.1:n.*531A>G
ENST00000703267.1:c.*794A>G (GUCA1ANB-GUCA1A)	ENSP00000515252.1:n.*794A>G
ENST00000372958.2:c.296A>G (GUCA1A) MANE Select	ENSP00000362049.1:p.Tyr99Cys
ENST00000394237.6:c.*794A>G (CIMIP3)	ENSP00000377784.2:n.*794A>G
ENST00000654459.1:c.296A>G (GUCA1A)	ENSP00000499539.1:p.Tyr99Cys
ENST00000659095.1:c.*531A>G (CIMIP3)	ENSP00000499714.1:n.*531A>G
ENST00000679182.1:c.77A>G (GUCA1A)	ENSP00000504837.1:p.Tyr26Cys
ENST00000053469.8:c.296A>G (GUCA1A)	ENSP00000053469.4:p.Tyr99Cys
ENST00000372958.1:c.296A>G (GUCA1A)	ENSP00000362049.1:p.Tyr99Cys
ENST00000394237.5:c.296A>G (GUCA1A)	ENSP00000377784.1:p.Tyr99Cys
ENST00000541991.5:c.284A>G (GUCA1A)	ENSP00000437476.2:p.Tyr95Cys
NM_000409.3:c.296A>G (GUCA1A)	NP_000400.2:p.Tyr99Cys
XM_006715073.2:c.77A>G (GUCA1A)	XP_006715136.1:p.Tyr26Cys
XM_011514536.1:c.296A>G (GUCA1A)	XP_011512838.1:p.Tyr99Cys
XM_011514537.1:c.296A>G (GUCA1A)	XP_011512839.1:p.Tyr99Cys
XM_011514538.1:c.296A>G (GUCA1A)	XP_011512840.1:p.Tyr99Cys
XM_011514539.1:c.296A>G (GUCA1A)	XP_011512841.1:p.Tyr99Cys
NM_000409.4:c.296A>G (GUCA1A)	NP_000400.2:p.Tyr99Cys
NM_001319061.1:c.296A>G (GUCA1A)	NP_001305990.1:p.Tyr99Cys
NM_001319062.1:c.296A>G (GUCA1A)	NP_001305991.1:p.Tyr99Cys
XM_006715073.3:c.77A>G (GUCA1A)	XP_006715136.1:p.Tyr26Cys
XM_011514537.2:c.296A>G (GUCA1A)	XP_011512839.1:p.Tyr99Cys
NM_000409.5:c.296A>G (GUCA1A)	NP_000400.2:p.Tyr99Cys
NM_001319061.2:c.296A>G (GUCA1A)	NP_001305990.1:p.Tyr99Cys
NM_001319062.2:c.296A>G (GUCA1A)	NP_001305991.1:p.Tyr99Cys
NM_001384910.1:c.296A>G (GUCA1A) MANE Select	NP_001371839.1:p.Tyr99Cys