Canonical Allele Identifier: CA415119709

Gene: HCFC1

Linked Data

• dbSNP Id: rs1557113997
• gnomAD v2: X-153220125-A-G
• gnomAD v4: X-153954674-A-G
• MyVariant Identifiers: chrX:g.153220125A>G (hg19) ; chrX:g.153954674A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153954674A>G , CM000685.2:g.153954674A>G	GRCh38
NC_000023.10:g.153220125A>G , CM000685.1:g.153220125A>G	GRCh37
NC_000023.9:g.152873319A>G	NCBI36
NG_012513.1:g.21695T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310441.12:c.3725T>C MANE Select	ENSP00000309555.7:p.Met1242Thr
ENST00000310441.11:c.3725T>C	ENSP00000309555.7:p.Met1242Thr
ENST00000369984.4:c.3725T>C	ENSP00000359001.4:p.Met1242Thr
NM_005334.2:c.3725T>C	NP_005325.2:p.Met1242Thr
XM_006724815.1:c.3725T>C	XP_006724878.1:p.Met1242Thr
XM_006724816.1:c.3725T>C	XP_006724879.1:p.Met1242Thr
XM_011531144.1:c.3725T>C	XP_011529446.1:p.Met1242Thr
XM_011531145.1:c.3725T>C	XP_011529447.1:p.Met1242Thr
XM_011531146.1:c.3725T>C	XP_011529448.1:p.Met1242Thr
XM_011531147.1:c.3725T>C	XP_011529449.1:p.Met1242Thr
XM_011531148.1:c.3725T>C	XP_011529450.1:p.Met1242Thr
XM_011531149.1:c.3527T>C	XP_011529451.1:p.Met1176Thr
XM_011531150.1:c.2816T>C	XP_011529452.1:p.Met939Thr
XM_006724815.3:c.3725T>C	XP_006724878.1:p.Met1242Thr
XM_006724816.3:c.3725T>C	XP_006724879.1:p.Met1242Thr
XM_011531147.3:c.3725T>C	XP_011529449.1:p.Met1242Thr
XM_011531148.3:c.3725T>C	XP_011529450.1:p.Met1242Thr
XM_017029471.2:c.3527T>C	XP_016884960.1:p.Met1176Thr
XM_017029472.1:c.2816T>C	XP_016884961.1:p.Met939Thr
NM_005334.3:c.3725T>C MANE Select	NP_005325.2:p.Met1242Thr