Canonical Allele Identifier: CA440226454

Linked Data

MyVariant Identifiers: chr4:g.79832941A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911787A>C , CM000666.2:g.78911787A>C GRCh38
NC_000004.11:g.79832941A>C , CM000666.1:g.79832941A>C GRCh37
NC_000004.10:g.80051965A>C NCBI36
NG_047162.1:g.140410A>C
NG_053104.1:g.32652T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.3240A>C (BMP2K) MANE Select ENSP00000424668.2:p.Ser1080=
ENST00000335016.9:c.3240A>C (BMP2K) ENSP00000334836.5:p.Ser1080=
ENST00000342820.10:c.*782+3423T>G (PAQR3) ENSP00000344203.6:n.*782+3423T>G
ENST00000502613.1:c.2317A>C (BMP2K)
ENST00000511594.5:c.*402T>G (PAQR3) ENSP00000425080.1:n.*402T>G
ENST00000512760.5:c.*792+3423T>G (PAQR3) ENSP00000426875.1:n.*792+3423T>G
ENST00000628286.1:c.*2216A>C (BMP2K) ENSP00000487317.1:n.*2216A>C
NM_198892.1:c.3240A>C (BMP2K) NP_942595.1:p.Ser1080=
XM_005263117.1:c.3129A>C (BMP2K) XP_005263174.1:p.Ser1043=
XM_011532101.1:c.3000A>C (BMP2K) XP_011530403.1:p.Ser1000=
XR_938694.1:n.1118-5626T>G (PAQR3)
XM_017008381.1:c.3000A>C (BMP2K) XP_016863870.1:p.Ser1000=
XM_017008382.1:c.2352A>C (BMP2K) XP_016863871.1:p.Ser784=
XR_938694.3:n.1098-5626T>G (PAQR3)
NM_198892.2:c.3240A>C (BMP2K) MANE Select NP_942595.1:p.Ser1080=