Canonical Allele Identifier: CA357404740

Linked Data

dbSNP Id: rs1243760371
gnomAD v2: 4-79832922-T-C
gnomAD v4: 4-78911768-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911768T>C , CM000666.2:g.78911768T>C GRCh38
NC_000004.11:g.79832922T>C , CM000666.1:g.79832922T>C GRCh37
NC_000004.10:g.80051946T>C NCBI36
NG_047162.1:g.140391T>C
NG_053104.1:g.32671A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.3221T>C (BMP2K) MANE Select ENSP00000424668.2:p.Phe1074Ser
ENST00000335016.9:c.3221T>C (BMP2K) ENSP00000334836.5:p.Phe1074Ser
ENST00000342820.10:c.*782+3442A>G (PAQR3) ENSP00000344203.6:n.*782+3442A>G
ENST00000502613.1:c.2298T>C (BMP2K)
ENST00000511594.5:c.*421A>G (PAQR3) ENSP00000425080.1:n.*421A>G
ENST00000512760.5:c.*792+3442A>G (PAQR3) ENSP00000426875.1:n.*792+3442A>G
ENST00000628286.1:c.*2197T>C (BMP2K) ENSP00000487317.1:n.*2197T>C
NM_198892.1:c.3221T>C (BMP2K) NP_942595.1:p.Phe1074Ser
XM_005263117.1:c.3110T>C (BMP2K) XP_005263174.1:p.Phe1037Ser
XM_011532101.1:c.2981T>C (BMP2K) XP_011530403.1:p.Phe994Ser
XR_938694.1:n.1118-5607A>G (PAQR3)
XM_017008381.1:c.2981T>C (BMP2K) XP_016863870.1:p.Phe994Ser
XM_017008382.1:c.2333T>C (BMP2K) XP_016863871.1:p.Phe778Ser
XR_938694.3:n.1098-5607A>G (PAQR3)
NM_198892.2:c.3221T>C (BMP2K) MANE Select NP_942595.1:p.Phe1074Ser