Canonical Allele Identifier: CA130179762

Gene: ADAM19

Linked Data

• dbSNP Id: rs577074316
• gnomAD v3: 5-157505430-A-G
• gnomAD v4: 5-157505430-A-G
• MyVariant Identifiers: chr5:g.156932438A>G (hg19) ; chr5:g.157505430A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157505430A>G , CM000667.2:g.157505430A>G	GRCh38
NC_000005.9:g.156932438A>G , CM000667.1:g.156932438A>G	GRCh37
NC_000005.8:g.156865016A>G	NCBI36
NG_046960.1:g.75394T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000257527.9:c.1130+239T>C MANE Select	ENSP00000257527.5:n.1130+239T>C
ENST00000257527.8:c.1130+239T>C	ENSP00000257527.4:n.1130+239T>C
ENST00000517905.1:c.1130+239T>C	ENSP00000428654.1:n.1130+239T>C
ENST00000517951.5:c.*321+239T>C	ENSP00000428376.1:n.*321+239T>C
NM_033274.4:c.1130+239T>C	NP_150377.1:n.1130+239T>C
XM_005266003.2:c.1130+239T>C	XP_005266060.1:n.1130+239T>C
XM_011534680.1:c.329+239T>C	XP_011532982.1:n.329+239T>C
XM_011534681.1:c.329+239T>C	XP_011532983.1:n.329+239T>C
XM_011534682.1:c.329+239T>C	XP_011532984.1:n.329+239T>C
XM_011534682.2:c.329+239T>C	XP_011532984.1:n.329+239T>C
XM_017010009.1:c.329+239T>C	XP_016865498.1:n.329+239T>C
NM_033274.5:c.1130+239T>C MANE Select	NP_150377.1:n.1130+239T>C