Canonical Allele Identifier: CA361984006

Gene: ADAM19

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157509354A>C , CM000667.2:g.157509354A>C	GRCh38
NC_000005.9:g.156936362A>C , CM000667.1:g.156936362A>C	GRCh37
NC_000005.8:g.156868940A>C	NCBI36
NG_046960.1:g.71470T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.852T>G MANE Select	ENSP00000257527.5:p.Ser284Arg
ENST00000257527.8:c.852T>G	ENSP00000257527.4:p.Ser284Arg
ENST00000517905.1:c.852T>G	ENSP00000428654.1:p.Ser284Arg
ENST00000517951.5:c.*43T>G	ENSP00000428376.1:n.*43T>G
NM_033274.4:c.852T>G	NP_150377.1:p.Ser284Arg
XM_005266003.2:c.852T>G	XP_005266060.1:p.Ser284Arg
XM_011534680.1:c.51T>G	XP_011532982.1:p.Ser17Arg
XM_011534681.1:c.51T>G	XP_011532983.1:p.Ser17Arg
XM_011534682.1:c.51T>G	XP_011532984.1:p.Ser17Arg
XM_011534682.2:c.51T>G	XP_011532984.1:p.Ser17Arg
XM_017010009.1:c.51T>G	XP_016865498.1:p.Ser17Arg
NM_033274.5:c.852T>G MANE Select	NP_150377.1:p.Ser284Arg