Canonical Allele Identifier: CA1541398948

Gene: C7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40979660_40979661delinsAT , CM000667.2:g.40979660_40979661delinsAT	GRCh38
NC_000005.9:g.40979762_40979763delinsAT , CM000667.1:g.40979762_40979763delinsAT	GRCh37
NC_000005.8:g.41015519_41015520delinsAT	NCBI36
NG_011692.1:g.75164_75165delinsAT , LRG_30:g.75164_75165delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696333.1:c.2166-65_2166-64delinsAT	ENSP00000512566.1:n.2166-65_2166-64delinsAT
ENST00000696441.1:c.2166-65_2166-64delinsAT	ENSP00000512631.1:n.2166-65_2166-64delinsAT
ENST00000696442.1:n.100-65_100-64delinsAT
ENST00000706664.1:n.2280-65_2280-64delinsAT
ENST00000706666.1:n.2241+2820_2241+2821delinsAT
ENST00000706667.1:n.3056-65_3056-64delinsAT
ENST00000706668.1:n.2894-65_2894-64delinsAT
ENST00000313164.10:c.2166-65_2166-64delinsAT MANE Select	ENSP00000322061.9:n.2166-65_2166-64delinsAT
ENST00000313164.9:c.2166-65_2166-64delinsAT	ENSP00000322061.9:n.2166-65_2166-64delinsAT
ENST00000464864.1:n.179-65_179-64delinsAT
ENST00000494960.5:n.166-65_166-64delinsAT
NM_000587.2:c.2166-65_2166-64delinsAT , LRG_30t1:c.2166-65_2166-64delinsAT	NP_000578.2:n.2166-65_2166-64delinsAT
XM_011514122.1:c.2166-65_2166-64delinsAT	XP_011512424.1:n.2166-65_2166-64delinsAT
NM_000587.3:c.2166-65_2166-64delinsAT	NP_000578.2:n.2166-65_2166-64delinsAT
NM_000587.4:c.2166-65_2166-64delinsAT MANE Select	NP_000578.2:n.2166-65_2166-64delinsAT