Canonical Allele Identifier: CA1879767497

Gene: GARNL3

Linked Data

• dbSNP Id: rs7029536

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127348132C>G , CM000671.2:g.127348132C>G	GRCh38
NC_000009.11:g.130110411C>G , CM000671.1:g.130110411C>G	GRCh37
NC_000009.10:g.129150232C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373387.9:c.1432-792C>G MANE Select	ENSP00000362485.4:n.1432-792C>G
ENST00000373386.6:c.1378-792C>G	ENSP00000362484.2:n.1378-792C>G
ENST00000373387.8:c.1432-792C>G	ENSP00000362485.4:n.1432-792C>G
ENST00000435213.6:c.1366-792C>G	ENSP00000396205.2:n.1366-792C>G
ENST00000460176.6:c.200+2655C>G
NM_001286779.1:c.1366-792C>G	NP_001273708.1:n.1366-792C>G
NM_032293.4:c.1432-792C>G	NP_115669.3:n.1432-792C>G
NR_104591.1:n.1833-792C>G
XM_005252267.2:c.1621-792C>G	XP_005252324.1:n.1621-792C>G
XM_005252268.1:c.1501-792C>G	XP_005252325.1:n.1501-792C>G
XM_011519086.1:c.1579-792C>G	XP_011517388.1:n.1579-792C>G
XM_011519087.1:c.1579-792C>G	XP_011517389.1:n.1579-792C>G
XM_011519088.1:c.1579-792C>G	XP_011517390.1:n.1579-792C>G
XM_011519089.1:c.1501-792C>G	XP_011517391.1:n.1501-792C>G
XM_011519090.1:c.925-792C>G	XP_011517392.1:n.925-792C>G
XM_005252267.3:c.1621-792C>G	XP_005252324.1:n.1621-792C>G
XM_005252268.2:c.1501-792C>G	XP_005252325.1:n.1501-792C>G
XM_011519086.3:c.1579-792C>G	XP_011517388.1:n.1579-792C>G
XM_011519087.2:c.1579-792C>G	XP_011517389.1:n.1579-792C>G
XM_011519089.3:c.1501-792C>G	XP_011517391.1:n.1501-792C>G
XM_011519090.2:c.925-792C>G	XP_011517392.1:n.925-792C>G
XM_017015202.1:c.1474-792C>G	XP_016870691.1:n.1474-792C>G
XM_024447693.1:c.1501-792C>G	XP_024303461.1:n.1501-792C>G
XM_024447694.1:c.925-792C>G	XP_024303462.1:n.925-792C>G
XM_024447695.1:c.925-792C>G	XP_024303463.1:n.925-792C>G
XM_024447696.1:c.925-792C>G	XP_024303464.1:n.925-792C>G
XM_024447697.1:c.925-792C>G	XP_024303465.1:n.925-792C>G
XR_001746389.1:n.1687+2655C>G
NM_032293.5:c.1432-792C>G MANE Select	NP_115669.3:n.1432-792C>G
NM_001286779.2:c.1366-792C>G	NP_001273708.1:n.1366-792C>G
NR_104591.2:n.1536-792C>G