Canonical Allele Identifier: CA440226401

Linked Data

MyVariant Identifiers: chr4:g.79832902C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911748C>T , CM000666.2:g.78911748C>T GRCh38
NC_000004.11:g.79832902C>T , CM000666.1:g.79832902C>T GRCh37
NC_000004.10:g.80051926C>T NCBI36
NG_047162.1:g.140371C>T
NG_053104.1:g.32691G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.3201C>T (BMP2K) MANE Select ENSP00000424668.2:p.Asp1067=
ENST00000335016.9:c.3201C>T (BMP2K) ENSP00000334836.5:p.Asp1067=
ENST00000342820.10:c.*782+3462G>A (PAQR3) ENSP00000344203.6:n.*782+3462G>A
ENST00000502613.1:c.2278C>T (BMP2K)
ENST00000511594.5:c.*441G>A (PAQR3) ENSP00000425080.1:n.*441G>A
ENST00000512760.5:c.*792+3462G>A (PAQR3) ENSP00000426875.1:n.*792+3462G>A
ENST00000628286.1:c.*2177C>T (BMP2K) ENSP00000487317.1:n.*2177C>T
NM_198892.1:c.3201C>T (BMP2K) NP_942595.1:p.Asp1067=
XM_005263117.1:c.3090C>T (BMP2K) XP_005263174.1:p.Asp1030=
XM_011532101.1:c.2961C>T (BMP2K) XP_011530403.1:p.Asp987=
XR_938694.1:n.1118-5587G>A (PAQR3)
XM_017008381.1:c.2961C>T (BMP2K) XP_016863870.1:p.Asp987=
XM_017008382.1:c.2313C>T (BMP2K) XP_016863871.1:p.Asp771=
XR_938694.3:n.1098-5587G>A (PAQR3)
NM_198892.2:c.3201C>T (BMP2K) MANE Select NP_942595.1:p.Asp1067=