Canonical Allele Identifier: CA415119901

Gene: HCFC1

Linked Data

• ClinVar Variation Id: 1028362
• ClinVar RCV Id: RCV001329391
• dbSNP Id: rs2065355018
• MyVariant Identifiers: chrX:g.153220176A>G (hg19) ; chrX:g.153954725A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153954725A>G , CM000685.2:g.153954725A>G	GRCh38
NC_000023.10:g.153220176A>G , CM000685.1:g.153220176A>G	GRCh37
NC_000023.9:g.152873370A>G	NCBI36
NG_012513.1:g.21644T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310441.12:c.3674T>C MANE Select	ENSP00000309555.7:p.Ile1225Thr
ENST00000310441.11:c.3674T>C	ENSP00000309555.7:p.Ile1225Thr
ENST00000369984.4:c.3674T>C	ENSP00000359001.4:p.Ile1225Thr
NM_005334.2:c.3674T>C	NP_005325.2:p.Ile1225Thr
XM_006724815.1:c.3674T>C	XP_006724878.1:p.Ile1225Thr
XM_006724816.1:c.3674T>C	XP_006724879.1:p.Ile1225Thr
XM_011531144.1:c.3674T>C	XP_011529446.1:p.Ile1225Thr
XM_011531145.1:c.3674T>C	XP_011529447.1:p.Ile1225Thr
XM_011531146.1:c.3674T>C	XP_011529448.1:p.Ile1225Thr
XM_011531147.1:c.3674T>C	XP_011529449.1:p.Ile1225Thr
XM_011531148.1:c.3674T>C	XP_011529450.1:p.Ile1225Thr
XM_011531149.1:c.3476T>C	XP_011529451.1:p.Ile1159Thr
XM_011531150.1:c.2765T>C	XP_011529452.1:p.Ile922Thr
XM_006724815.3:c.3674T>C	XP_006724878.1:p.Ile1225Thr
XM_006724816.3:c.3674T>C	XP_006724879.1:p.Ile1225Thr
XM_011531147.3:c.3674T>C	XP_011529449.1:p.Ile1225Thr
XM_011531148.3:c.3674T>C	XP_011529450.1:p.Ile1225Thr
XM_017029471.2:c.3476T>C	XP_016884960.1:p.Ile1159Thr
XM_017029472.1:c.2765T>C	XP_016884961.1:p.Ile922Thr
NM_005334.3:c.3674T>C MANE Select	NP_005325.2:p.Ile1225Thr