Canonical Allele Identifier: CA2654931779

Gene: SLC19A1

Linked Data

• gnomAD v4: 21-45544484-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45544484G>T , CM000683.2:g.45544484G>T	GRCh38
NC_000021.8:g.46964398G>T , CM000683.1:g.46964398G>T	GRCh37
NC_000021.7:g.45788826G>T	NCBI36
NG_028278.1:g.2988C>A
NG_028278.2:g.23660C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000650808.1:c.-49-6476C>A	ENSP00000498221.1:n.-49-6476C>A
XM_011529696.1:c.17C>A	XP_011527998.1:p.Pro6Gln
XM_011529697.1:c.17C>A	XP_011527999.1:p.Pro6Gln
XM_011529700.1:c.-49-6476C>A	XP_011528002.1:n.-49-6476C>A
XM_011529705.1:c.17C>A	XP_011528007.1:p.Pro6Gln
XM_011529707.1:c.17C>A	XP_011528009.1:p.Pro6Gln
XM_011529708.1:c.-270C>A	XP_011528010.1:n.-270C>A
XM_011529709.1:c.-407-6476C>A	XP_011528011.1:n.-407-6476C>A
XM_011529710.1:c.-165-12336C>A	XP_011528012.1:n.-165-12336C>A
NM_001352511.1:c.-49-6476C>A	NP_001339440.1:n.-49-6476C>A
XM_011529696.2:c.17C>A	XP_011527998.1:p.Pro6Gln
XM_011529700.2:c.-49-6476C>A	XP_011528002.1:n.-49-6476C>A
XM_011529709.2:c.-407-6476C>A	XP_011528011.1:n.-407-6476C>A
XM_017028444.1:c.17C>A	XP_016883933.1:p.Pro6Gln
XM_017028445.2:c.17C>A	XP_016883934.1:p.Pro6Gln
NM_001352511.2:c.-49-6476C>A	NP_001339440.1:n.-49-6476C>A
NM_001352511.3:c.-49-6476C>A	NP_001339440.1:n.-49-6476C>A