Canonical Allele Identifier: CA497383773

Gene: GEMIN4

Linked Data

• MyVariant Identifiers: chr17:g.649339T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.746099T>G , CM000679.2:g.746099T>G	GRCh38
NC_000017.10:g.649339T>G , CM000679.1:g.649339T>G	GRCh37
NC_000017.9:g.596089T>G	NCBI36
NG_046938.1:g.11774A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319004.6:c.1944A>C MANE Select	ENSP00000321706.5:p.Pro648=
ENST00000319004.5:c.1944A>C	ENSP00000321706.5:p.Pro648=
ENST00000576778.1:c.1911A>C	ENSP00000459565.1:p.Pro637=
NM_015721.2:c.1944A>C	NP_056536.2:p.Pro648=
XM_005256667.3:c.1956A>C	XP_005256724.1:p.Pro652=
XM_005256668.3:c.1956A>C	XP_005256725.1:p.Pro652=
XM_005256670.3:c.1911A>C	XP_005256727.1:p.Pro637=
XM_011523910.1:c.1956A>C	XP_011522212.1:p.Pro652=
XM_011523911.1:c.1956A>C	XP_011522213.1:p.Pro652=
XM_011523912.1:c.1911A>C	XP_011522214.1:p.Pro637=
XM_011523913.1:c.1911A>C	XP_011522215.1:p.Pro637=
XM_005256667.4:c.1956A>C	XP_005256724.1:p.Pro652=
XM_005256670.5:c.1911A>C	XP_005256727.1:p.Pro637=
XM_011523910.2:c.1956A>C	XP_011522212.1:p.Pro652=
XM_011523911.2:c.1956A>C	XP_011522213.1:p.Pro652=
XM_011523912.2:c.1911A>C	XP_011522214.1:p.Pro637=
XM_011523913.2:c.1911A>C	XP_011522215.1:p.Pro637=
XM_017024709.1:c.1956A>C	XP_016880198.1:p.Pro652=
NM_015721.3:c.1944A>C MANE Select	NP_056536.2:p.Pro648=