Canonical Allele Identifier: CA2392214127

Gene: SLC19A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45544403G= , CM000683.2:g.45544403G=	GRCh38
NC_000021.8:g.46964317G= , CM000683.1:g.46964317G=	GRCh37
NC_000021.7:g.45788745G=	NCBI36
NG_028278.1:g.3069C=
NG_028278.2:g.23741C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650808.1:c.-49-6395C=	ENSP00000498221.1:n.-49-6395C=
ENST00000567670.5:c.-316C=	ENSP00000457278.1:n.-316C=
XM_011529696.1:c.33-57C=	XP_011527998.1:n.33-57C=
XM_011529697.1:c.33-57C=	XP_011527999.1:n.33-57C=
XM_011529700.1:c.-49-6395C=	XP_011528002.1:n.-49-6395C=
XM_011529705.1:c.33-57C=	XP_011528007.1:n.33-57C=
XM_011529707.1:c.33-57C=	XP_011528009.1:n.33-57C=
XM_011529708.1:c.-254-62C=	XP_011528010.1:n.-254-62C=
XM_011529709.1:c.-407-6395C=	XP_011528011.1:n.-407-6395C=
XM_011529710.1:c.-165-12255C=	XP_011528012.1:n.-165-12255C=
NM_001352511.1:c.-49-6395C=	NP_001339440.1:n.-49-6395C=
XM_011529696.2:c.33-57C=	XP_011527998.1:n.33-57C=
XM_011529700.2:c.-49-6395C=	XP_011528002.1:n.-49-6395C=
XM_011529709.2:c.-407-6395C=	XP_011528011.1:n.-407-6395C=
XM_017028444.1:c.33-57C=	XP_016883933.1:n.33-57C=
XM_017028445.2:c.33-57C=	XP_016883934.1:n.33-57C=
NM_001352511.2:c.-49-6395C=	NP_001339440.1:n.-49-6395C=
NM_001352511.3:c.-49-6395C=	NP_001339440.1:n.-49-6395C=