Canonical Allele Identifier: CA384045029

Gene: ETV6

Linked Data

• MyVariant Identifiers: chr12:g.12038957T>C (hg19) ; chr12:g.11886023T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11886023T>C , CM000674.2:g.11886023T>C	GRCh38
NC_000012.11:g.12038957T>C , CM000674.1:g.12038957T>C	GRCh37
NC_000012.10:g.11930224T>C	NCBI36
NG_011443.1:g.241170T>C , LRG_609:g.241170T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1250T>C MANE Select	ENSP00000379658.3:p.Phe417Ser
ENST00000266427.3:c.87T>C
ENST00000396373.8:c.1250T>C	ENSP00000379658.3:p.Phe417Ser
NM_001987.4:c.1250T>C , LRG_609t1:c.1250T>C	NP_001978.1:p.Phe417Ser
XM_011520607.1:c.1247T>C	XP_011518909.1:p.Phe416Ser
XM_011520608.1:c.1223T>C	XP_011518910.1:p.Phe408Ser
XM_011520609.1:c.986T>C	XP_011518911.1:p.Phe329Ser
XM_011520610.1:c.986T>C	XP_011518912.1:p.Phe329Ser
XM_011520611.1:c.986T>C	XP_011518913.1:p.Phe329Ser
XM_011520612.1:c.629T>C	XP_011518914.1:p.Phe210Ser
XM_011520607.2:c.1247T>C	XP_011518909.1:p.Phe416Ser
XM_011520608.2:c.1223T>C	XP_011518910.1:p.Phe408Ser
XM_011520609.2:c.986T>C	XP_011518911.1:p.Phe329Ser
XM_011520611.2:c.986T>C	XP_011518913.1:p.Phe329Ser
XM_011520612.2:c.629T>C	XP_011518914.1:p.Phe210Ser
XM_017018990.1:c.1115T>C	XP_016874479.1:p.Phe372Ser
XM_017018991.1:c.986T>C	XP_016874480.1:p.Phe329Ser
NM_001987.5:c.1250T>C MANE Select	NP_001978.1:p.Phe417Ser