Canonical Allele Identifier: CA404850258

Gene: CRLF1

Linked Data

• MyVariant Identifiers: chr19:g.18705167T>G (hg19) ; chr19:g.18594357T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18594357T>G , CM000681.2:g.18594357T>G	GRCh38
NC_000019.9:g.18705167T>G , CM000681.1:g.18705167T>G	GRCh37
NC_000019.8:g.18566167T>G	NCBI36
NG_013370.1:g.17494A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684169.1:c.1102A>C	ENSP00000506849.1:p.Lys368Gln
ENST00000392386.8:c.1102A>C MANE Select	ENSP00000376188.2:p.Lys368Gln
ENST00000392386.7:c.1102A>C	ENSP00000376188.2:p.Lys368Gln
ENST00000594325.1:n.79A>C
NM_004750.4:c.1102A>C	NP_004741.1:p.Lys368Gln
XM_011528422.1:c.1036A>C	XP_011526724.1:p.Lys346Gln
XM_011528423.1:c.1102A>C	XP_011526725.1:p.Lys368Gln
XM_011528424.1:c.1036A>C	XP_011526726.1:p.Lys346Gln
XM_011528422.2:c.1036A>C	XP_011526724.1:p.Lys346Gln
XM_011528423.2:c.1102A>C	XP_011526725.1:p.Lys368Gln
XM_011528424.3:c.1036A>C	XP_011526726.1:p.Lys346Gln
NM_004750.5:c.1102A>C MANE Select	NP_004741.1:p.Lys368Gln