Canonical Allele Identifier: CA2638262005

Gene: GFAP

Linked Data

• gnomAD v4: 17-44908180-G-GCCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908180_44908181insCCCT , CM000679.2:g.44908180_44908181insCCCT	GRCh38
NC_000017.10:g.42985548_42985549insCCCT , CM000679.1:g.42985548_42985549insCCCT	GRCh37
NC_000017.9:g.40341074_40341075insCCCT	NCBI36
NG_008401.1:g.12366_12367insAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1292-32_1292-31insAGGG	ENSP00000253408.5:n.1292-32_1292-31insAGGG
ENST00000253408.10:c.1292-32_1292-31insAGGG	ENSP00000253408.5:n.1292-32_1292-31insAGGG
ENST00000441312.2:n.25-32_25-31insAGGG
ENST00000585543.6:n.325-32_325-31insAGGG
ENST00000586125.2:c.107-32_107-31insAGGG	ENSP00000467397.2:n.107-32_107-31insAGGG
ENST00000588735.3:c.1172-32_1172-31insAGGG MANE Select	ENSP00000466598.2:n.1172-32_1172-31insAGGG
ENST00000589701.2:n.2047_2048insAGGG
ENST00000591880.2:c.271-32_271-31insAGGG
ENST00000592065.2:n.508_509insAGGG
ENST00000638304.1:c.91-32_91-31insAGGG
ENST00000638400.1:c.7-32_7-31insAGGG
ENST00000638488.1:n.636-32_636-31insAGGG
ENST00000638618.1:c.827-32_827-31insAGGG	ENSP00000492832.1:n.827-32_827-31insAGGG
ENST00000638921.1:n.67_68insAGGG
ENST00000639042.1:c.144-32_144-31insAGGG
ENST00000639277.1:c.1172-32_1172-31insAGGG	ENSP00000492432.1:n.1172-32_1172-31insAGGG
ENST00000639369.1:c.22-32_22-31insAGGG
ENST00000253408.9:c.1172-32_1172-31insAGGG	ENSP00000253408.4:n.1172-32_1172-31insAGGG
ENST00000585543.5:n.325-32_325-31insAGGG
ENST00000586125.1:c.143-32_143-31insAGGG	ENSP00000467397.1:n.143-32_143-31insAGGG
ENST00000588640.5:n.552-32_552-31insAGGG
ENST00000588735.1:c.83-65_83-64insAGGG	ENSP00000466598.1:n.83-65_83-64insAGGG
ENST00000589701.1:n.42_43insAGGG
ENST00000591880.1:c.38-32_38-31insAGGG	ENSP00000467530.1:n.38-32_38-31insAGGG
ENST00000592706.5:n.44-32_44-31insAGGG
NM_002055.4:c.1172-32_1172-31insAGGG	NP_002046.1:n.1172-32_1172-31insAGGG
NM_001363846.1:c.1292-32_1292-31insAGGG	NP_001350775.1:n.1292-32_1292-31insAGGG
XM_024450690.1:c.1496-32_1496-31insAGGG	XP_024306458.1:n.1496-32_1496-31insAGGG
XM_024450692.1:c.1376-32_1376-31insAGGG	XP_024306460.1:n.1376-32_1376-31insAGGG
NM_002055.5:c.1172-32_1172-31insAGGG MANE Select	NP_002046.1:n.1172-32_1172-31insAGGG
NM_001363846.2:c.1292-32_1292-31insAGGG	NP_001350775.1:n.1292-32_1292-31insAGGG