Canonical Allele Identifier: CA397506340

Gene: GEMIN4

Linked Data

• dbSNP Id: rs1162861502
• gnomAD v2: 17-649482-T-C
• gnomAD v4: 17-746242-T-C
• MyVariant Identifiers: chr17:g.649482T>C (hg19) ; chr17:g.746242T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.746242T>C , CM000679.2:g.746242T>C	GRCh38
NC_000017.10:g.649482T>C , CM000679.1:g.649482T>C	GRCh37
NC_000017.9:g.596232T>C	NCBI36
NG_046938.1:g.11631A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319004.6:c.1801A>G MANE Select	ENSP00000321706.5:p.Thr601Ala
ENST00000319004.5:c.1801A>G	ENSP00000321706.5:p.Thr601Ala
ENST00000576778.1:c.1768A>G	ENSP00000459565.1:p.Thr590Ala
NM_015721.2:c.1801A>G	NP_056536.2:p.Thr601Ala
XM_005256667.3:c.1813A>G	XP_005256724.1:p.Thr605Ala
XM_005256668.3:c.1813A>G	XP_005256725.1:p.Thr605Ala
XM_005256670.3:c.1768A>G	XP_005256727.1:p.Thr590Ala
XM_011523910.1:c.1813A>G	XP_011522212.1:p.Thr605Ala
XM_011523911.1:c.1813A>G	XP_011522213.1:p.Thr605Ala
XM_011523912.1:c.1768A>G	XP_011522214.1:p.Thr590Ala
XM_011523913.1:c.1768A>G	XP_011522215.1:p.Thr590Ala
XM_005256667.4:c.1813A>G	XP_005256724.1:p.Thr605Ala
XM_005256670.5:c.1768A>G	XP_005256727.1:p.Thr590Ala
XM_011523910.2:c.1813A>G	XP_011522212.1:p.Thr605Ala
XM_011523911.2:c.1813A>G	XP_011522213.1:p.Thr605Ala
XM_011523912.2:c.1768A>G	XP_011522214.1:p.Thr590Ala
XM_011523913.2:c.1768A>G	XP_011522215.1:p.Thr590Ala
XM_017024709.1:c.1813A>G	XP_016880198.1:p.Thr605Ala
NM_015721.3:c.1801A>G MANE Select	NP_056536.2:p.Thr601Ala