Canonical Allele Identifier: CA380315544

Gene: SLC39A13

Linked Data

• MyVariant Identifiers: chr11:g.47436883T>C (hg19) ; chr11:g.47415332T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415332T>C , CM000673.2:g.47415332T>C	GRCh38
NC_000011.9:g.47436883T>C , CM000673.1:g.47436883T>C	GRCh37
NC_000011.8:g.47393459T>C	NCBI36
NG_017073.1:g.11838T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000362021.9:c.1085T>C MANE Select	ENSP00000354689.4:p.Val362Ala
ENST00000354884.8:c.1064T>C	ENSP00000346956.4:p.Val355Ala
ENST00000362021.8:c.1085T>C	ENSP00000354689.4:p.Val362Ala
ENST00000524886.1:n.343T>C
ENST00000524928.1:c.*1415T>C	ENSP00000437186.1:n.*1415T>C
ENST00000527829.1:n.445T>C
ENST00000533076.5:c.*82T>C	ENSP00000434290.1:n.*82T>C
NM_001128225.2:c.1085T>C	NP_001121697.1:p.Val362Ala
NM_152264.4:c.1064T>C	NP_689477.2:p.Val355Ala
XM_006718381.2:c.1109T>C	XP_006718444.1:p.Val370Ala
XM_006718383.2:c.1001T>C	XP_006718446.1:p.Val334Ala
XM_006718384.2:c.*82T>C	XP_006718447.1:n.*82T>C
XM_006718385.2:c.*82T>C	XP_006718448.1:n.*82T>C
XM_011520466.1:c.1130T>C	XP_011518768.1:p.Val377Ala
XM_011520467.1:c.1085T>C	XP_011518769.1:p.Val362Ala
XM_011520468.1:c.1085T>C	XP_011518770.1:p.Val362Ala
XM_011520469.1:c.1022T>C	XP_011518771.1:p.Val341Ala
XM_011520470.1:c.977T>C	XP_011518772.1:p.Val326Ala
XR_242832.1:n.1470T>C
XR_428862.2:n.1145T>C
XR_428863.2:n.1141T>C
XR_930928.1:n.1166T>C
NM_001330245.1:c.*82T>C	NP_001317174.1:n.*82T>C
NR_134854.1:n.1326T>C
XM_006718381.3:c.1109T>C	XP_006718444.1:p.Val370Ala
XM_006718383.3:c.1001T>C	XP_006718446.1:p.Val334Ala
XM_011520468.3:c.1085T>C	XP_011518770.1:p.Val362Ala
XM_011520470.2:c.977T>C	XP_011518772.1:p.Val326Ala
XM_017018540.2:c.1064T>C	XP_016874029.1:p.Val355Ala
XM_017018541.2:c.956T>C	XP_016874030.1:p.Val319Ala
XM_024448762.1:c.1214T>C	XP_024304530.1:p.Val405Ala
XR_001748027.1:n.1285T>C
XR_001748028.1:n.1267T>C
XR_428862.3:n.1145T>C
XR_428863.3:n.1141T>C
XR_930928.2:n.1166T>C
NM_001128225.3:c.1085T>C MANE Select	NP_001121697.2:p.Val362Ala
NM_001330245.2:c.*82T>C	NP_001317174.2:n.*82T>C
NM_152264.5:c.1064T>C	NP_689477.3:p.Val355Ala