Canonical Allele Identifier: CA2739239539

Gene: HCFC1

Linked Data

• dbSNP Id: rs2148572652

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153954826_153954846del , CM000685.2:g.153954826_153954846del	GRCh38
NC_000023.10:g.153220277_153220297del , CM000685.1:g.153220277_153220297del	GRCh37
NC_000023.9:g.152873471_152873491del	NCBI36
NG_012513.1:g.21523_21543del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310441.12:c.3553_3573del MANE Select	ENSP00000309555.7:p.Ala1185_Pro1191del
ENST00000310441.11:c.3553_3573del	ENSP00000309555.7:p.Ala1185_Pro1191del
ENST00000369984.4:c.3553_3573del	ENSP00000359001.4:p.Ala1185_Pro1191del
NM_005334.2:c.3553_3573del	NP_005325.2:p.Ala1185_Pro1191del
XM_006724815.1:c.3553_3573del	XP_006724878.1:p.Ala1185_Pro1191del
XM_006724816.1:c.3553_3573del	XP_006724879.1:p.Ala1185_Pro1191del
XM_011531144.1:c.3553_3573del	XP_011529446.1:p.Ala1185_Pro1191del
XM_011531145.1:c.3553_3573del	XP_011529447.1:p.Ala1185_Pro1191del
XM_011531146.1:c.3553_3573del	XP_011529448.1:p.Ala1185_Pro1191del
XM_011531147.1:c.3553_3573del	XP_011529449.1:p.Ala1185_Pro1191del
XM_011531148.1:c.3553_3573del	XP_011529450.1:p.Ala1185_Pro1191del
XM_011531149.1:c.3355_3375del	XP_011529451.1:p.Ala1119_Pro1125del
XM_011531150.1:c.2644_2664del	XP_011529452.1:p.Ala882_Pro888del
XM_006724815.3:c.3553_3573del	XP_006724878.1:p.Ala1185_Pro1191del
XM_006724816.3:c.3553_3573del	XP_006724879.1:p.Ala1185_Pro1191del
XM_011531147.3:c.3553_3573del	XP_011529449.1:p.Ala1185_Pro1191del
XM_011531148.3:c.3553_3573del	XP_011529450.1:p.Ala1185_Pro1191del
XM_017029471.2:c.3355_3375del	XP_016884960.1:p.Ala1119_Pro1125del
XM_017029472.1:c.2644_2664del	XP_016884961.1:p.Ala882_Pro888del
NM_005334.3:c.3553_3573del MANE Select	NP_005325.2:p.Ala1185_Pro1191del