Canonical Allele Identifier: CA806227450

Gene: ADAM19

Linked Data

• dbSNP Id: rs1399189037
• MyVariant Identifiers: chr5:g.156932322T>C (hg19) ; chr5:g.157505314T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157505314T>C , CM000667.2:g.157505314T>C	GRCh38
NC_000005.9:g.156932322T>C , CM000667.1:g.156932322T>C	GRCh37
NC_000005.8:g.156864900T>C	NCBI36
NG_046960.1:g.75510A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000257527.9:c.1130+355A>G MANE Select	ENSP00000257527.5:n.1130+355A>G
ENST00000257527.8:c.1130+355A>G	ENSP00000257527.4:n.1130+355A>G
ENST00000517905.1:c.1130+355A>G	ENSP00000428654.1:n.1130+355A>G
ENST00000517951.5:c.*321+355A>G	ENSP00000428376.1:n.*321+355A>G
NM_033274.4:c.1130+355A>G	NP_150377.1:n.1130+355A>G
XM_005266003.2:c.1130+355A>G	XP_005266060.1:n.1130+355A>G
XM_011534680.1:c.329+355A>G	XP_011532982.1:n.329+355A>G
XM_011534681.1:c.329+355A>G	XP_011532983.1:n.329+355A>G
XM_011534682.1:c.329+355A>G	XP_011532984.1:n.329+355A>G
XM_011534682.2:c.329+355A>G	XP_011532984.1:n.329+355A>G
XM_017010009.1:c.329+355A>G	XP_016865498.1:n.329+355A>G
NM_033274.5:c.1130+355A>G MANE Select	NP_150377.1:n.1130+355A>G