Canonical Allele Identifier: CA471625116

Gene: SFXN4

Linked Data

• MyVariant Identifiers: chr10:g.120907295A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119147783A>G , CM000672.2:g.119147783A>G	GRCh38
NC_000010.10:g.120907295A>G , CM000672.1:g.120907295A>G	GRCh37
NC_000010.9:g.120897285A>G	NCBI36
NG_033895.1:g.22910T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355697.7:c.810T>C MANE Select	ENSP00000347924.2:p.Phe270=
ENST00000355697.6:c.810T>C	ENSP00000347924.2:p.Phe270=
ENST00000369131.8:c.462T>C	ENSP00000358127.4:p.Phe154=
ENST00000461438.5:n.839T>C
ENST00000466218.5:n.759T>C
ENST00000484960.5:n.140T>C
ENST00000490417.6:n.273T>C
NM_213649.1:c.810T>C	NP_998814.1:p.Phe270=
NR_110305.1:n.828T>C
XM_005269525.3:c.783T>C	XP_005269582.1:p.Phe261=
XM_005269526.1:c.462T>C	XP_005269583.1:p.Phe154=
XM_005269527.1:c.462T>C	XP_005269584.1:p.Phe154=
XM_011539282.1:c.462T>C	XP_011537584.1:p.Phe154=
XR_945603.1:n.872T>C
XM_005269525.5:c.783T>C	XP_005269582.1:p.Phe261=
XM_005269526.2:c.462T>C	XP_005269583.1:p.Phe154=
XM_011539282.2:c.462T>C	XP_011537584.1:p.Phe154=
XM_024447793.1:c.462T>C	XP_024303561.1:p.Phe154=
XR_001747022.1:n.1061T>C
XR_001747023.1:n.955T>C
XR_945603.3:n.891T>C
NM_213649.2:c.810T>C MANE Select	NP_998814.1:p.Phe270=