Canonical Allele Identifier: CA2625142784

Gene: SLC38A6

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61050408G>T , CM000676.2:g.61050408G>T	GRCh38
NC_000014.8:g.61517126G>T , CM000676.1:g.61517126G>T	GRCh37
NC_000014.7:g.60586879G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703134.1:c.838+4241G>T	ENSP00000515189.1:n.838+4241G>T
ENST00000267488.9:c.926-104G>T MANE Select	ENSP00000267488.4:n.926-104G>T
ENST00000267488.8:c.926-104G>T	ENSP00000267488.4:n.926-104G>T
ENST00000354886.6:c.926-104G>T	ENSP00000346959.2:n.926-104G>T
ENST00000451406.5:c.911-104G>T	ENSP00000395851.1:n.911-104G>T
ENST00000491344.7:c.*800-104G>T	ENSP00000431212.2:n.*800-104G>T
ENST00000525723.6:c.*1210-104G>T	ENSP00000431260.2:n.*1210-104G>T
ENST00000526539.2:c.209-104G>T	ENSP00000450996.1:n.209-104G>T
ENST00000527591.5:c.1228-104G>T	ENSP00000434737.1:n.1228-104G>T
ENST00000529212.1:c.245-104G>T	ENSP00000437190.1:n.245-104G>T
ENST00000529345.6:c.1069-104G>T
NM_001172702.1:c.926-104G>T	NP_001166173.1:n.926-104G>T
NM_153811.2:c.926-104G>T	NP_722518.2:n.926-104G>T
NR_033344.1:n.1266-104G>T
XM_006720046.1:c.872-104G>T	XP_006720109.1:n.872-104G>T
XM_006720047.2:c.857-104G>T	XP_006720110.1:n.857-104G>T
XM_006720050.1:c.323-104G>T	XP_006720113.1:n.323-104G>T
XM_011536470.1:c.*19-104G>T	XP_011534772.1:n.*19-104G>T
XR_943394.1:n.1103-104G>T
XM_006720050.2:c.323-104G>T	XP_006720113.1:n.323-104G>T
XM_017021020.1:c.926-104G>T	XP_016876509.1:n.926-104G>T
XM_017021021.1:c.872-104G>T	XP_016876510.1:n.872-104G>T
XM_017021022.1:c.857-104G>T	XP_016876511.1:n.857-104G>T
XM_017021023.1:c.926-104G>T	XP_016876512.1:n.926-104G>T
XM_017021024.1:c.806-104G>T	XP_016876513.1:n.806-104G>T
XM_017021025.1:c.764-104G>T	XP_016876514.1:n.764-104G>T
XM_017021026.1:c.764-104G>T	XP_016876515.1:n.764-104G>T
XM_024449486.1:c.521-104G>T	XP_024305254.1:n.521-104G>T
XM_024449487.1:c.521-104G>T	XP_024305255.1:n.521-104G>T
XM_024449488.1:c.521-104G>T	XP_024305256.1:n.521-104G>T
XM_024449489.1:c.521-104G>T	XP_024305257.1:n.521-104G>T
XM_024449490.1:c.521-104G>T	XP_024305258.1:n.521-104G>T
XM_024449491.1:c.521-104G>T	XP_024305259.1:n.521-104G>T
XM_024449492.1:c.521-104G>T	XP_024305260.1:n.521-104G>T
XM_024449493.1:c.467-104G>T	XP_024305261.1:n.467-104G>T
XM_024449494.1:c.323-104G>T	XP_024305262.1:n.323-104G>T
XM_024449495.1:c.323-104G>T	XP_024305263.1:n.323-104G>T
XM_024449496.1:c.323-104G>T	XP_024305264.1:n.323-104G>T
XM_024449497.1:c.323-104G>T	XP_024305265.1:n.323-104G>T
XR_001750163.1:n.1092-104G>T
XR_001750164.1:n.1128-104G>T
XR_002957534.1:n.1189-104G>T
NR_033344.2:n.1268-104G>T
NM_001172702.2:c.926-104G>T	NP_001166173.1:n.926-104G>T
NM_153811.3:c.926-104G>T MANE Select	NP_722518.2:n.926-104G>T