Canonical Allele Identifier: CA7888719

Gene: NAGPA

Linked Data

• dbSNP Id: rs766738531
• ExAC: 16:5079058 T / G
• gnomAD v2: 16-5079058-T-G
• gnomAD v4: 16-5029057-T-G
• MyVariant Identifiers: chr16:g.5079058T>G (hg19) ; chr16:g.5029057T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5029057T>G , CM000678.2:g.5029057T>G	GRCh38
NC_000016.9:g.5079058T>G , CM000678.1:g.5079058T>G	GRCh37
NC_000016.8:g.5019059T>G	NCBI36
NG_028152.1:g.9885A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.792-49A>C MANE Select	ENSP00000310998.3:n.792-49A>C
ENST00000649828.1:c.792-49A>C	ENSP00000498032.1:n.792-49A>C
ENST00000312251.7:c.792-49A>C	ENSP00000310998.3:n.792-49A>C
ENST00000381955.7:c.792-49A>C	ENSP00000371381.3:n.792-49A>C
ENST00000562037.1:c.553-49A>C	ENSP00000464994.1:n.553-49A>C
ENST00000562346.2:c.505-872A>C
ENST00000562746.5:c.792-49A>C	ENSP00000455900.1:n.792-49A>C
ENST00000563578.5:c.610-49A>C
ENST00000564397.5:n.1102A>C
ENST00000565876.5:c.480+1328A>C
ENST00000567739.5:n.62A>C
ENST00000568202.5:n.655-49A>C
ENST00000569296.5:c.336-49A>C	ENSP00000465949.1:n.336-49A>C
NM_016256.3:c.792-49A>C	NP_057340.2:n.792-49A>C
XM_011522517.1:c.792-49A>C	XP_011520819.1:n.792-49A>C
XM_011522518.1:c.792-49A>C	XP_011520820.1:n.792-49A>C
XM_011522519.1:c.792-49A>C	XP_011520821.1:n.792-49A>C
XR_243285.1:n.819-49A>C
XM_011522517.3:c.792-49A>C	XP_011520819.1:n.792-49A>C
XR_001751908.2:n.818-49A>C
XR_001751909.2:n.818-49A>C
XR_001751910.2:n.818-49A>C
XR_001751911.2:n.818-49A>C
XR_001751912.2:n.818-49A>C
NM_016256.4:c.792-49A>C MANE Select	NP_057340.2:n.792-49A>C