Canonical Allele Identifier: CA357402081

Linked Data

gnomAD v4: 4-78911335-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911335G>A , CM000666.2:g.78911335G>A GRCh38
NC_000004.11:g.79832489G>A , CM000666.1:g.79832489G>A GRCh37
NC_000004.10:g.80051513G>A NCBI36
NG_047162.1:g.139958G>A
NG_053104.1:g.33104C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2788G>A (BMP2K) MANE Select ENSP00000424668.2:p.Asp930Asn
ENST00000335016.9:c.2788G>A (BMP2K) ENSP00000334836.5:p.Asp930Asn
ENST00000342820.10:c.*782+3875C>T (PAQR3) ENSP00000344203.6:n.*782+3875C>T
ENST00000502613.1:c.1865G>A (BMP2K)
ENST00000511594.5:c.*854C>T (PAQR3) ENSP00000425080.1:n.*854C>T
ENST00000512760.5:c.*792+3875C>T (PAQR3) ENSP00000426875.1:n.*792+3875C>T
ENST00000628286.1:c.*1764G>A (BMP2K) ENSP00000487317.1:n.*1764G>A
NM_198892.1:c.2788G>A (BMP2K) NP_942595.1:p.Asp930Asn
XM_005263117.1:c.2677G>A (BMP2K) XP_005263174.1:p.Asp893Asn
XM_011532101.1:c.2548G>A (BMP2K) XP_011530403.1:p.Asp850Asn
XR_938694.1:n.1118-5174C>T (PAQR3)
XM_017008381.1:c.2548G>A (BMP2K) XP_016863870.1:p.Asp850Asn
XM_017008382.1:c.1900G>A (BMP2K) XP_016863871.1:p.Asp634Asn
XR_938694.3:n.1098-5174C>T (PAQR3)
NM_198892.2:c.2788G>A (BMP2K) MANE Select NP_942595.1:p.Asp930Asn