Canonical Allele Identifier: CA440226140

Linked Data

MyVariant Identifiers: chr4:g.79832671C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911517C>T , CM000666.2:g.78911517C>T GRCh38
NC_000004.11:g.79832671C>T , CM000666.1:g.79832671C>T GRCh37
NC_000004.10:g.80051695C>T NCBI36
NG_047162.1:g.140140C>T
NG_053104.1:g.32922G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2970C>T (BMP2K) MANE Select ENSP00000424668.2:p.Ser990=
ENST00000335016.9:c.2970C>T (BMP2K) ENSP00000334836.5:p.Ser990=
ENST00000342820.10:c.*782+3693G>A (PAQR3) ENSP00000344203.6:n.*782+3693G>A
ENST00000502613.1:c.2047C>T (BMP2K)
ENST00000511594.5:c.*672G>A (PAQR3) ENSP00000425080.1:n.*672G>A
ENST00000512760.5:c.*792+3693G>A (PAQR3) ENSP00000426875.1:n.*792+3693G>A
ENST00000628286.1:c.*1946C>T (BMP2K) ENSP00000487317.1:n.*1946C>T
NM_198892.1:c.2970C>T (BMP2K) NP_942595.1:p.Ser990=
XM_005263117.1:c.2859C>T (BMP2K) XP_005263174.1:p.Ser953=
XM_011532101.1:c.2730C>T (BMP2K) XP_011530403.1:p.Ser910=
XR_938694.1:n.1118-5356G>A (PAQR3)
XM_017008381.1:c.2730C>T (BMP2K) XP_016863870.1:p.Ser910=
XM_017008382.1:c.2082C>T (BMP2K) XP_016863871.1:p.Ser694=
XR_938694.3:n.1098-5356G>A (PAQR3)
NM_198892.2:c.2970C>T (BMP2K) MANE Select NP_942595.1:p.Ser990=