Canonical Allele Identifier: CA497383938
Gene: GEMIN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.649237C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.745997C>A , CM000679.2:g.745997C>A GRCh38
NC_000017.10:g.649237C>A , CM000679.1:g.649237C>A GRCh37
NC_000017.9:g.595987C>A NCBI36
NG_046938.1:g.11876G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000319004.6:c.2046G>T MANE Select ENSP00000321706.5:p.Ala682=
ENST00000319004.5:c.2046G>T ENSP00000321706.5:p.Ala682=
ENST00000576778.1:c.2013G>T ENSP00000459565.1:p.Ala671=
NM_015721.2:c.2046G>T NP_056536.2:p.Ala682=
XM_005256667.3:c.2058G>T XP_005256724.1:p.Ala686=
XM_005256668.3:c.2058G>T XP_005256725.1:p.Ala686=
XM_005256670.3:c.2013G>T XP_005256727.1:p.Ala671=
XM_011523910.1:c.2058G>T XP_011522212.1:p.Ala686=
XM_011523911.1:c.2058G>T XP_011522213.1:p.Ala686=
XM_011523912.1:c.2013G>T XP_011522214.1:p.Ala671=
XM_011523913.1:c.2013G>T XP_011522215.1:p.Ala671=
XM_005256667.4:c.2058G>T XP_005256724.1:p.Ala686=
XM_005256670.5:c.2013G>T XP_005256727.1:p.Ala671=
XM_011523910.2:c.2058G>T XP_011522212.1:p.Ala686=
XM_011523911.2:c.2058G>T XP_011522213.1:p.Ala686=
XM_011523912.2:c.2013G>T XP_011522214.1:p.Ala671=
XM_011523913.2:c.2013G>T XP_011522215.1:p.Ala671=
XM_017024709.1:c.2058G>T XP_016880198.1:p.Ala686=
NM_015721.3:c.2046G>T MANE Select NP_056536.2:p.Ala682=