Canonical Allele Identifier: CA1769215101

Gene: SLC18A1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20180955T= , CM000670.2:g.20180955T=	GRCh38
NC_000008.10:g.20038466T= , CM000670.1:g.20038466T=	GRCh37
NC_000008.9:g.20082746T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003053.4:c.10A= MANE Select	NP_003044.1:p.Thr4=
ENST00000276373.10:c.10A= MANE Select	ENSP00000276373.5:p.Thr4=
NM_001135691.2:c.10A=	NP_001129163.1:p.Thr4=
NM_001135691.3:c.10A=	NP_001129163.1:p.Thr4=
NM_001142324.1:c.10A=	NP_001135796.1:p.Thr4=
NM_001142324.2:c.10A=	NP_001135796.1:p.Thr4=
NM_001142325.1:c.10A=	NP_001135797.1:p.Thr4=
NM_001142325.2:c.10A=	NP_001135797.1:p.Thr4=
NM_003053.3:c.10A=	NP_003044.1:p.Thr4=
ENST00000265808.11:c.10A=	ENSP00000265808.7:p.Thr4=
ENST00000276373.9:c.10A=	ENSP00000276373.5:p.Thr4=
ENST00000381608.8:c.10A=	ENSP00000371021.4:p.Thr4=
ENST00000437980.3:c.10A=	ENSP00000413361.1:p.Thr4=
ENST00000440926.3:c.10A=	ENSP00000387549.1:p.Thr4=
ENST00000517776.5:c.10A=	ENSP00000428001.1:p.Thr4=
ENST00000519026.5:c.10A=	ENSP00000429664.1:p.Thr4=
ENST00000522513.5:c.10A=	ENSP00000428999.1:p.Thr4=
XM_011544623.1:c.10A=	XP_011542925.1:p.Thr4=
XM_011544624.1:c.10A=	XP_011542926.1:p.Thr4=
XM_011544625.1:c.10A=	XP_011542927.1:p.Thr4=
XM_011544626.1:c.10A=	XP_011542928.1:p.Thr4=
XM_011544627.1:c.10A=	XP_011542929.1:p.Thr4=
XM_011544628.1:c.10A=	XP_011542930.1:p.Thr4=