Canonical Allele Identifier: CA519702008

Gene: HCFC1

Linked Data

• MyVariant Identifiers: chrX:g.153219974T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153954523T>C , CM000685.2:g.153954523T>C	GRCh38
NC_000023.10:g.153219974T>C , CM000685.1:g.153219974T>C	GRCh37
NC_000023.9:g.152873168T>C	NCBI36
NG_012513.1:g.21846A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310441.12:c.3876A>G MANE Select	ENSP00000309555.7:p.Pro1292=
ENST00000310441.11:c.3876A>G	ENSP00000309555.7:p.Pro1292=
ENST00000369984.4:c.3876A>G	ENSP00000359001.4:p.Pro1292=
NM_005334.2:c.3876A>G	NP_005325.2:p.Pro1292=
XM_006724815.1:c.3876A>G	XP_006724878.1:p.Pro1292=
XM_006724816.1:c.3876A>G	XP_006724879.1:p.Pro1292=
XM_011531144.1:c.3876A>G	XP_011529446.1:p.Pro1292=
XM_011531145.1:c.3876A>G	XP_011529447.1:p.Pro1292=
XM_011531146.1:c.3876A>G	XP_011529448.1:p.Pro1292=
XM_011531147.1:c.3876A>G	XP_011529449.1:p.Pro1292=
XM_011531148.1:c.3876A>G	XP_011529450.1:p.Pro1292=
XM_011531149.1:c.3678A>G	XP_011529451.1:p.Pro1226=
XM_011531150.1:c.2967A>G	XP_011529452.1:p.Pro989=
XM_006724815.3:c.3876A>G	XP_006724878.1:p.Pro1292=
XM_006724816.3:c.3876A>G	XP_006724879.1:p.Pro1292=
XM_011531147.3:c.3876A>G	XP_011529449.1:p.Pro1292=
XM_011531148.3:c.3876A>G	XP_011529450.1:p.Pro1292=
XM_017029471.2:c.3678A>G	XP_016884960.1:p.Pro1226=
XM_017029472.1:c.2967A>G	XP_016884961.1:p.Pro989=
NM_005334.3:c.3876A>G MANE Select	NP_005325.2:p.Pro1292=