Canonical Allele Identifier: CA1627477871

Gene: RHAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619040_49619044delinsCCATT , CM000668.2:g.49619040_49619044delinsCCATT	GRCh38
NC_000006.11:g.49586753_49586757delinsCCATT , CM000668.1:g.49586753_49586757delinsCCATT	GRCh37
NC_000006.10:g.49694712_49694716delinsCCATT	NCBI36
NG_011704.1:g.22831_22835delinsAATGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.341+135_341+139delinsAATGG MANE Select	ENSP00000360217.4:n.341+135_341+139delinsAATGG
ENST00000642530.1:n.616+135_616+139delinsAATGG
ENST00000646272.1:c.341+135_341+139delinsAATGG	ENSP00000494337.1:n.341+135_341+139delinsAATGG
ENST00000646939.1:c.341+135_341+139delinsAATGG	ENSP00000494709.1:n.341+135_341+139delinsAATGG
ENST00000646963.1:c.341+135_341+139delinsAATGG	ENSP00000495337.1:n.341+135_341+139delinsAATGG
ENST00000229810.9:c.341+135_341+139delinsAATGG	ENSP00000229810.8:n.341+135_341+139delinsAATGG
ENST00000371175.8:c.341+135_341+139delinsAATGG	ENSP00000360217.4:n.341+135_341+139delinsAATGG
ENST00000618248.3:c.341+135_341+139delinsAATGG	ENSP00000482984.1:n.341+135_341+139delinsAATGG
NM_000324.2:c.341+135_341+139delinsAATGG	NP_000315.2:n.341+135_341+139delinsAATGG
XM_011514788.1:c.341+135_341+139delinsAATGG	XP_011513090.1:n.341+135_341+139delinsAATGG
NM_000324.3:c.341+135_341+139delinsAATGG MANE Select	NP_000315.2:n.341+135_341+139delinsAATGG