Canonical Allele Identifier: CA404850889

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18596938-G-T
• MyVariant Identifiers: chr19:g.18707748G>T (hg19) ; chr19:g.18596938G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596938G>T , CM000681.2:g.18596938G>T	GRCh38
NC_000019.9:g.18707748G>T , CM000681.1:g.18707748G>T	GRCh37
NC_000019.8:g.18568748G>T	NCBI36
NG_013370.1:g.14913C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.809C>A	ENSP00000506849.1:p.Ala270Asp
ENST00000392386.8:c.809C>A MANE Select	ENSP00000376188.2:p.Ala270Asp
ENST00000392386.7:c.809C>A	ENSP00000376188.2:p.Ala270Asp
ENST00000597131.1:c.274C>A
NM_004750.4:c.809C>A	NP_004741.1:p.Ala270Asp
XM_011528422.1:c.743C>A	XP_011526724.1:p.Ala248Asp
XM_011528423.1:c.809C>A	XP_011526725.1:p.Ala270Asp
XM_011528424.1:c.743C>A	XP_011526726.1:p.Ala248Asp
XM_011528422.2:c.743C>A	XP_011526724.1:p.Ala248Asp
XM_011528423.2:c.809C>A	XP_011526725.1:p.Ala270Asp
XM_011528424.3:c.743C>A	XP_011526726.1:p.Ala248Asp
NM_004750.5:c.809C>A MANE Select	NP_004741.1:p.Ala270Asp