Canonical Allele Identifier: CA8262519
Gene: GEMIN4 HGNC NCBI

Linked Data

dbSNP Id: rs776310179

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.746109_746111del , CM000679.2:g.746109_746111del GRCh38
NC_000017.10:g.649349_649351del , CM000679.1:g.649349_649351del GRCh37
NC_000017.9:g.596099_596101del NCBI36
NG_046938.1:g.11766_11768del

Transcript Alleles

HGVS Amino-acid Change
ENST00000319004.6:c.1936_1938del MANE Select ENSP00000321706.5:p.Leu646del
ENST00000319004.5:c.1936_1938del ENSP00000321706.5:p.Leu646del
ENST00000576778.1:c.1903_1905del ENSP00000459565.1:p.Leu635del
NM_015721.2:c.1936_1938del NP_056536.2:p.Leu646del
XM_005256667.3:c.1948_1950del XP_005256724.1:p.Leu650del
XM_005256668.3:c.1948_1950del XP_005256725.1:p.Leu650del
XM_005256670.3:c.1903_1905del XP_005256727.1:p.Leu635del
XM_011523910.1:c.1948_1950del XP_011522212.1:p.Leu650del
XM_011523911.1:c.1948_1950del XP_011522213.1:p.Leu650del
XM_011523912.1:c.1903_1905del XP_011522214.1:p.Leu635del
XM_011523913.1:c.1903_1905del XP_011522215.1:p.Leu635del
XM_005256667.4:c.1948_1950del XP_005256724.1:p.Leu650del
XM_005256670.5:c.1903_1905del XP_005256727.1:p.Leu635del
XM_011523910.2:c.1948_1950del XP_011522212.1:p.Leu650del
XM_011523911.2:c.1948_1950del XP_011522213.1:p.Leu650del
XM_011523912.2:c.1903_1905del XP_011522214.1:p.Leu635del
XM_011523913.2:c.1903_1905del XP_011522215.1:p.Leu635del
XM_017024709.1:c.1948_1950del XP_016880198.1:p.Leu650del
NM_015721.3:c.1936_1938del MANE Select NP_056536.2:p.Leu646del