Canonical Allele Identifier: CA414502394

Gene: SLITRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.145823546C>G , CM000685.2:g.145823546C>G	GRCh38
NC_000023.10:g.144905064C>G , CM000685.1:g.144905064C>G	GRCh37
NC_000023.9:g.144712756C>G	NCBI36
NG_016477.1:g.10718C>G
NG_016553.1:g.1137C>G
NG_016477.2:g.10718C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032539.5:c.1121C>G MANE Select	NP_115928.1:p.Pro374Arg
ENST00000335565.6:c.1121C>G MANE Select	ENSP00000334374.5:p.Pro374Arg
NM_001144003.2:c.1121C>G	NP_001137475.1:p.Pro374Arg
NM_001144003.3:c.1121C>G	NP_001137475.1:p.Pro374Arg
NM_001144004.2:c.1121C>G	NP_001137476.1:p.Pro374Arg
NM_001144004.3:c.1121C>G	NP_001137476.1:p.Pro374Arg
NM_001144005.2:c.1121C>G	NP_001137477.1:p.Pro374Arg
NM_001144005.3:c.1121C>G	NP_001137477.1:p.Pro374Arg
NM_001144006.2:c.1121C>G	NP_001137478.1:p.Pro374Arg
NM_001144008.2:c.1121C>G	NP_001137480.1:p.Pro374Arg
NM_001144009.2:c.1121C>G	NP_001137481.1:p.Pro374Arg
NM_001144010.2:c.1121C>G	NP_001137482.1:p.Pro374Arg
NM_032539.4:c.1121C>G	NP_115928.1:p.Pro374Arg
ENST00000335565.4:c.1121C>G	ENSP00000334374.4:p.Pro374Arg
ENST00000370490.1:c.1121C>G	ENSP00000359521.1:p.Pro374Arg
XM_005262342.2:c.1121C>G	XP_005262399.1:p.Pro374Arg
XM_005262342.3:c.1121C>G	XP_005262399.1:p.Pro374Arg
XM_005262343.2:c.1121C>G	XP_005262400.1:p.Pro374Arg
XM_005262343.3:c.1121C>G	XP_005262400.1:p.Pro374Arg
XM_005262344.2:c.1121C>G	XP_005262401.1:p.Pro374Arg
XM_005262344.3:c.1121C>G	XP_005262401.1:p.Pro374Arg
XM_005262345.2:c.1121C>G	XP_005262402.1:p.Pro374Arg
XM_005262345.3:c.1121C>G	XP_005262402.1:p.Pro374Arg