Canonical Allele Identifier: CA357404853

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911819T>G , CM000666.2:g.78911819T>G GRCh38
NC_000004.11:g.79832973T>G , CM000666.1:g.79832973T>G GRCh37
NC_000004.10:g.80051997T>G NCBI36
NG_047162.1:g.140442T>G
NG_053104.1:g.32620A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.3272T>G (BMP2K) MANE Select ENSP00000424668.2:p.Ile1091Ser
ENST00000335016.9:c.3272T>G (BMP2K) ENSP00000334836.5:p.Ile1091Ser
ENST00000342820.10:c.*782+3391A>C (PAQR3) ENSP00000344203.6:n.*782+3391A>C
ENST00000502613.1:c.2349T>G (BMP2K)
ENST00000511594.5:c.*370A>C (PAQR3) ENSP00000425080.1:n.*370A>C
ENST00000512760.5:c.*792+3391A>C (PAQR3) ENSP00000426875.1:n.*792+3391A>C
ENST00000628286.1:c.*2248T>G (BMP2K) ENSP00000487317.1:n.*2248T>G
NM_198892.1:c.3272T>G (BMP2K) NP_942595.1:p.Ile1091Ser
XM_005263117.1:c.3161T>G (BMP2K) XP_005263174.1:p.Ile1054Ser
XM_011532101.1:c.3032T>G (BMP2K) XP_011530403.1:p.Ile1011Ser
XR_938694.1:n.1118-5658A>C (PAQR3)
XM_017008381.1:c.3032T>G (BMP2K) XP_016863870.1:p.Ile1011Ser
XM_017008382.1:c.2384T>G (BMP2K) XP_016863871.1:p.Ile795Ser
XR_938694.3:n.1098-5658A>C (PAQR3)
NM_198892.2:c.3272T>G (BMP2K) MANE Select NP_942595.1:p.Ile1091Ser