Canonical Allele Identifier: CA2770997865
Gene: RHAG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49619385_49619386insAAACCAAACACACCCAACACA , CM000668.2:g.49619385_49619386insAAACCAAACACACCCAACACA GRCh38
NC_000006.11:g.49587098_49587099insAAACCAAACACACCCAACACA , CM000668.1:g.49587098_49587099insAAACCAAACACACCCAACACA GRCh37
NC_000006.10:g.49695057_49695058insAAACCAAACACACCCAACACA NCBI36
NG_011704.1:g.22490_22491insGTGTTGGGTGTGTTTGGTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371175.10:c.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT MANE Select ENSP00000360217.4:n.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT
ENST00000642530.1:n.433-23_433-22insGTGTTGGGTGTGTTTGGTTTT
ENST00000646272.1:c.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT ENSP00000494337.1:n.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT
ENST00000646939.1:c.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT ENSP00000494709.1:n.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT
ENST00000646963.1:c.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT ENSP00000495337.1:n.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT
ENST00000229810.9:c.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT ENSP00000229810.8:n.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT
ENST00000371175.8:c.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT ENSP00000360217.4:n.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT
ENST00000618248.3:c.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT ENSP00000482984.1:n.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT
NM_000324.2:c.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT NP_000315.2:n.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT
XM_011514788.1:c.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT XP_011513090.1:n.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT
NM_000324.3:c.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT MANE Select NP_000315.2:n.158-23_158-22insGTGTTGGGTGTGTTTGGTTTT