Canonical Allele Identifier: CA13989321
Gene: SLC25A21 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36809759A>G , CM000676.2:g.36809759A>G GRCh38
NC_000014.8:g.37278964A>G , CM000676.1:g.37278964A>G GRCh37
NC_000014.7:g.36348715A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331299.6:c.203+4159T>C MANE Select ENSP00000329452.5:n.203+4159T>C
ENST00000331299.5:c.203+4159T>C ENSP00000329452.5:n.203+4159T>C
ENST00000555449.5:c.203+4159T>C ENSP00000451873.1:n.203+4159T>C
ENST00000622765.4:c.8+4159T>C ENSP00000481445.1:n.8+4159T>C
NM_001171170.1:c.203+4159T>C NP_001164641.1:n.203+4159T>C
NM_030631.3:c.203+4159T>C NP_085134.1:n.203+4159T>C
XM_011537287.1:c.215+4159T>C XP_011535589.1:n.215+4159T>C
XM_011537288.1:c.113+4159T>C XP_011535590.1:n.113+4159T>C
XM_011537289.1:c.-120+4159T>C XP_011535591.1:n.-120+4159T>C
XM_011537287.3:c.215+4159T>C XP_011535589.1:n.215+4159T>C
XM_011537288.3:c.113+4159T>C XP_011535590.1:n.113+4159T>C
XM_011537289.3:c.-120+4159T>C XP_011535591.1:n.-120+4159T>C
NM_001171170.2:c.203+4159T>C NP_001164641.1:n.203+4159T>C
NM_030631.4:c.203+4159T>C MANE Select NP_085134.1:n.203+4159T>C
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