Canonical Allele Identifier: CA1594194210

Gene: ADAM19

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157494947A>C , CM000667.2:g.157494947A>C	GRCh38
NC_000005.9:g.156921955A>C , CM000667.1:g.156921955A>C	GRCh37
NC_000005.8:g.156854533A>C	NCBI36
NG_046960.1:g.85877T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.1595-152T>G MANE Select	ENSP00000257527.5:n.1595-152T>G
ENST00000257527.8:c.1595-152T>G	ENSP00000257527.4:n.1595-152T>G
ENST00000517374.5:c.307-152T>G
ENST00000517905.1:c.1595-152T>G	ENSP00000428654.1:n.1595-152T>G
ENST00000517951.5:c.*786-152T>G	ENSP00000428376.1:n.*786-152T>G
NM_033274.4:c.1595-152T>G	NP_150377.1:n.1595-152T>G
XM_005266003.2:c.1595-152T>G	XP_005266060.1:n.1595-152T>G
XM_011534680.1:c.794-152T>G	XP_011532982.1:n.794-152T>G
XM_011534681.1:c.794-152T>G	XP_011532983.1:n.794-152T>G
XM_011534682.1:c.794-152T>G	XP_011532984.1:n.794-152T>G
XM_011534682.2:c.794-152T>G	XP_011532984.1:n.794-152T>G
XM_017010009.1:c.794-152T>G	XP_016865498.1:n.794-152T>G
NM_033274.5:c.1595-152T>G MANE Select	NP_150377.1:n.1595-152T>G