Canonical Allele Identifier: CA2611381697
Gene: ADAM12 HGNC NCBI

Linked Data

gnomAD v4: 10-126036117-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.126036117A>C , CM000672.2:g.126036117A>C GRCh38
NC_000010.10:g.127724686A>C , CM000672.1:g.127724686A>C GRCh37
NC_000010.9:g.127714676A>C NCBI36
NG_029050.1:g.357442T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000448723.2:c.2529+29T>G MANE Select ENSP00000391268.2:n.2529+29T>G
ENST00000368679.8:c.2538+29T>G ENSP00000357668.4:n.2538+29T>G
NM_001288973.1:c.2529+29T>G NP_001275902.1:n.2529+29T>G
NM_003474.5:c.2538+29T>G NP_003465.3:n.2538+29T>G
XM_017016705.1:c.2070+29T>G XP_016872194.1:n.2070+29T>G
XM_017016706.1:c.1371+29T>G XP_016872195.1:n.1371+29T>G
XM_024448210.1:c.1200+29T>G XP_024303978.1:n.1200+29T>G
NM_001288973.2:c.2529+29T>G MANE Select NP_001275902.1:n.2529+29T>G
NM_003474.6:c.2538+29T>G NP_003465.3:n.2538+29T>G
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