Canonical Allele Identifier: CA506044621

Gene: CRLF1

Linked Data

• MyVariant Identifiers: chr19:g.18710475G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18599665G>C , CM000681.2:g.18599665G>C	GRCh38
NC_000019.9:g.18710475G>C , CM000681.1:g.18710475G>C	GRCh37
NC_000019.8:g.18571475G>C	NCBI36
NG_013370.1:g.12186C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.297C>G	ENSP00000506849.1:p.Ala99=
ENST00000392386.8:c.297C>G MANE Select	ENSP00000376188.2:p.Ala99=
ENST00000392386.7:c.297C>G	ENSP00000376188.2:p.Ala99=
NM_004750.4:c.297C>G	NP_004741.1:p.Ala99=
XM_011528422.1:c.231C>G	XP_011526724.1:p.Ala77=
XM_011528423.1:c.297C>G	XP_011526725.1:p.Ala99=
XM_011528424.1:c.231C>G	XP_011526726.1:p.Ala77=
XM_011528422.2:c.231C>G	XP_011526724.1:p.Ala77=
XM_011528423.2:c.297C>G	XP_011526725.1:p.Ala99=
XM_011528424.3:c.231C>G	XP_011526726.1:p.Ala77=
NM_004750.5:c.297C>G MANE Select	NP_004741.1:p.Ala99=