Canonical Allele Identifier: CA15369727

Gene: ADAM19

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157525400C>G , CM000667.2:g.157525400C>G	GRCh38
NC_000005.9:g.156952408C>G , CM000667.1:g.156952408C>G	GRCh37
NC_000005.8:g.156884986C>G	NCBI36
NG_046960.1:g.55424G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.408-5369G>C MANE Select	ENSP00000257527.5:n.408-5369G>C
ENST00000257527.8:c.408-5369G>C	ENSP00000257527.4:n.408-5369G>C
ENST00000517905.1:c.408-5369G>C	ENSP00000428654.1:n.408-5369G>C
ENST00000517951.5:c.408-5369G>C	ENSP00000428376.1:n.408-5369G>C
NM_033274.4:c.408-5369G>C	NP_150377.1:n.408-5369G>C
XM_005266003.2:c.408-5369G>C	XP_005266060.1:n.408-5369G>C
XM_011534680.1:c.-136+5407G>C	XP_011532982.1:n.-136+5407G>C
XM_011534681.1:c.-146+5407G>C	XP_011532983.1:n.-146+5407G>C
NM_033274.5:c.408-5369G>C MANE Select	NP_150377.1:n.408-5369G>C