Canonical Allele Identifier: CA221691604

Gene: SLC39A13

Linked Data

• dbSNP Id: rs199651988
• gnomAD v2: 11-47436749-G-A
• gnomAD v4: 11-47415198-G-A
• MyVariant Identifiers: chr11:g.47436749G>A (hg19) ; chr11:g.47415198G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415198G>A , CM000673.2:g.47415198G>A	GRCh38
NC_000011.9:g.47436749G>A , CM000673.1:g.47436749G>A	GRCh37
NC_000011.8:g.47393325G>A	NCBI36
NG_017073.1:g.11704G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1040+39G>A MANE Select	ENSP00000354689.4:n.1040+39G>A
ENST00000354884.8:c.1019+39G>A	ENSP00000346956.4:n.1019+39G>A
ENST00000362021.8:c.1040+39G>A	ENSP00000354689.4:n.1040+39G>A
ENST00000524886.1:n.298+39G>A
ENST00000524928.1:c.*1281G>A	ENSP00000437186.1:n.*1281G>A
ENST00000527829.1:n.311G>A
ENST00000533076.5:c.*37+39G>A	ENSP00000434290.1:n.*37+39G>A
NM_001128225.2:c.1040+39G>A	NP_001121697.1:n.1040+39G>A
NM_152264.4:c.1019+39G>A	NP_689477.2:n.1019+39G>A
XM_006718381.2:c.1064+39G>A	XP_006718444.1:n.1064+39G>A
XM_006718383.2:c.956+39G>A	XP_006718446.1:n.956+39G>A
XM_006718384.2:c.*37+39G>A	XP_006718447.1:n.*37+39G>A
XM_006718385.2:c.*37+39G>A	XP_006718448.1:n.*37+39G>A
XM_011520466.1:c.1085+39G>A	XP_011518768.1:n.1085+39G>A
XM_011520467.1:c.1040+39G>A	XP_011518769.1:n.1040+39G>A
XM_011520468.1:c.1040+39G>A	XP_011518770.1:n.1040+39G>A
XM_011520469.1:c.977+39G>A	XP_011518771.1:n.977+39G>A
XM_011520470.1:c.932+39G>A	XP_011518772.1:n.932+39G>A
XR_242832.1:n.1425+39G>A
XR_428862.2:n.1100+39G>A
XR_428863.2:n.1096+39G>A
XR_930928.1:n.1121+39G>A
NM_001330245.1:c.*37+39G>A	NP_001317174.1:n.*37+39G>A
NR_134854.1:n.1281+39G>A
XM_006718381.3:c.1064+39G>A	XP_006718444.1:n.1064+39G>A
XM_006718383.3:c.956+39G>A	XP_006718446.1:n.956+39G>A
XM_011520468.3:c.1040+39G>A	XP_011518770.1:n.1040+39G>A
XM_011520470.2:c.932+39G>A	XP_011518772.1:n.932+39G>A
XM_017018540.2:c.1019+39G>A	XP_016874029.1:n.1019+39G>A
XM_017018541.2:c.911+39G>A	XP_016874030.1:n.911+39G>A
XM_024448762.1:c.1169+39G>A	XP_024304530.1:n.1169+39G>A
XR_001748027.1:n.1240+39G>A
XR_001748028.1:n.1222+39G>A
XR_428862.3:n.1100+39G>A
XR_428863.3:n.1096+39G>A
XR_930928.2:n.1121+39G>A
NM_001128225.3:c.1040+39G>A MANE Select	NP_001121697.2:n.1040+39G>A
NM_001330245.2:c.*37+39G>A	NP_001317174.2:n.*37+39G>A
NM_152264.5:c.1019+39G>A	NP_689477.3:n.1019+39G>A