Canonical Allele Identifier: CA16571291
Gene: SLC7A10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33223022C>T , CM000681.2:g.33223022C>T GRCh38
NC_000019.9:g.33713928C>T , CM000681.1:g.33713928C>T GRCh37
NC_000019.8:g.38405768C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253188.8:c.151+2531G>A MANE Select ENSP00000253188.2:n.151+2531G>A
ENST00000587064.5:c.151+2531G>A ENSP00000466876.1:n.151+2531G>A
ENST00000590036.5:c.151+2531G>A ENSP00000465421.1:n.151+2531G>A
ENST00000592596.1:c.151+2531G>A ENSP00000466410.1:n.151+2531G>A
NM_019849.2:c.151+2531G>A NP_062823.1:n.151+2531G>A
XM_006723284.2:c.151+2531G>A XP_006723347.1:n.151+2531G>A
XM_011527119.1:c.151+2531G>A XP_011525421.1:n.151+2531G>A
XM_011527120.1:c.275+2531G>A XP_011525422.1:n.275+2531G>A
XR_935841.1:n.170+2531G>A
XM_024451609.1:c.151+2531G>A XP_024307377.1:n.151+2531G>A
XM_024451610.1:c.275+2531G>A XP_024307378.1:n.275+2531G>A
NM_019849.3:c.151+2531G>A MANE Select NP_062823.1:n.151+2531G>A
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