Canonical Allele Identifier: CA2648593775

Gene: CRP

Linked Data

• gnomAD v4: 1-159713811-T-TCTACC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713813_159713817dup , CM000663.2:g.159713813_159713817dup	GRCh38
NC_000001.10:g.159683603_159683607dup , CM000663.1:g.159683603_159683607dup	GRCh37
NC_000001.9:g.157950227_157950231dup	NCBI36
NG_013007.1:g.5774_5778dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.384_388dup MANE Select	ENSP00000255030.5:p.Asp130GlyfsTer2
ENST00000368110.1:c.194-176_194-172dup	ENSP00000357091.1:n.194-176_194-172dup
ENST00000368111.5:c.194-176_194-172dup	ENSP00000357092.1:n.194-176_194-172dup
ENST00000368112.5:c.197+187_197+191dup	ENSP00000357093.1:n.197+187_197+191dup
ENST00000437342.1:c.-151_-147dup	ENSP00000402788.1:n.-151_-147dup
ENST00000489317.1:n.74+191_74+195dup
NM_000567.2:c.384_388dup	NP_000558.2:p.Asp130GlyfsTer2
XM_011509207.1:c.384_388dup	XP_011507509.1:p.Asp130GlyfsTer2
NM_001329057.1:c.384_388dup	NP_001315986.1:p.Asp130GlyfsTer2
NM_001329058.1:c.197+187_197+191dup	NP_001315987.1:n.197+187_197+191dup
NM_000567.3:c.384_388dup MANE Select	NP_000558.2:p.Asp130GlyfsTer2
NM_001329057.2:c.384_388dup	NP_001315986.1:p.Asp130GlyfsTer2
NM_001329058.2:c.197+187_197+191dup	NP_001315987.1:n.197+187_197+191dup
NM_001382703.1:c.194-176_194-172dup	NP_001369632.1:n.194-176_194-172dup