Canonical Allele Identifier: CA215377037

Gene: ADAM12

Linked Data

• dbSNP Id: rs945528828
• MyVariant Identifiers: chr10:g.126036122A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126036122A>C , CM000672.2:g.126036122A>C	GRCh38
NC_000010.10:g.127724691A>C , CM000672.1:g.127724691A>C	GRCh37
NC_000010.9:g.127714681A>C	NCBI36
NG_029050.1:g.357437T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000448723.2:c.2529+24T>G MANE Select	ENSP00000391268.2:n.2529+24T>G
ENST00000368679.8:c.2538+24T>G	ENSP00000357668.4:n.2538+24T>G
NM_001288973.1:c.2529+24T>G	NP_001275902.1:n.2529+24T>G
NM_003474.5:c.2538+24T>G	NP_003465.3:n.2538+24T>G
XM_017016705.1:c.2070+24T>G	XP_016872194.1:n.2070+24T>G
XM_017016706.1:c.1371+24T>G	XP_016872195.1:n.1371+24T>G
XM_024448210.1:c.1200+24T>G	XP_024303978.1:n.1200+24T>G
NM_001288973.2:c.2529+24T>G MANE Select	NP_001275902.1:n.2529+24T>G
NM_003474.6:c.2538+24T>G	NP_003465.3:n.2538+24T>G