Canonical Allele Identifier: CA2638262336

Gene: GFAP

Linked Data

• dbSNP Id: rs2145626644
• gnomAD v4: 17-44908227-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908227_44908228insA , CM000679.2:g.44908227_44908228insA	GRCh38
NC_000017.10:g.42985595_42985596insA , CM000679.1:g.42985595_42985596insA	GRCh37
NC_000017.9:g.40341121_40341122insA	NCBI36
NG_008401.1:g.12319_12320insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253408.11:c.1292-79_1292-78insT	ENSP00000253408.5:n.1292-79_1292-78insT
ENST00000253408.10:c.1292-79_1292-78insT	ENSP00000253408.5:n.1292-79_1292-78insT
ENST00000441312.2:n.25-79_25-78insT
ENST00000585543.6:n.325-79_325-78insT
ENST00000586125.2:c.107-79_107-78insT	ENSP00000467397.2:n.107-79_107-78insT
ENST00000588735.3:c.1172-79_1172-78insT MANE Select	ENSP00000466598.2:n.1172-79_1172-78insT
ENST00000589701.2:n.2000_2001insT
ENST00000591880.2:c.271-79_271-78insT
ENST00000592065.2:n.461_462insT
ENST00000638304.1:c.91-79_91-78insT
ENST00000638400.1:c.7-79_7-78insT
ENST00000638488.1:n.636-79_636-78insT
ENST00000638618.1:c.827-79_827-78insT	ENSP00000492832.1:n.827-79_827-78insT
ENST00000638921.1:n.20_21insT
ENST00000639042.1:c.144-79_144-78insT
ENST00000639277.1:c.1172-79_1172-78insT	ENSP00000492432.1:n.1172-79_1172-78insT
ENST00000639369.1:c.22-79_22-78insT
ENST00000640552.1:n.3572_3573insT
ENST00000253408.9:c.1172-79_1172-78insT	ENSP00000253408.4:n.1172-79_1172-78insT
ENST00000585543.5:n.325-79_325-78insT
ENST00000586125.1:c.143-79_143-78insT	ENSP00000467397.1:n.143-79_143-78insT
ENST00000588640.5:n.552-79_552-78insT
ENST00000588735.1:c.83-112_83-111insT	ENSP00000466598.1:n.83-112_83-111insT
ENST00000591880.1:c.38-79_38-78insT	ENSP00000467530.1:n.38-79_38-78insT
ENST00000592706.5:n.44-79_44-78insT
NM_002055.4:c.1172-79_1172-78insT	NP_002046.1:n.1172-79_1172-78insT
NM_001363846.1:c.1292-79_1292-78insT	NP_001350775.1:n.1292-79_1292-78insT
XM_024450690.1:c.1496-79_1496-78insT	XP_024306458.1:n.1496-79_1496-78insT
XM_024450692.1:c.1376-79_1376-78insT	XP_024306460.1:n.1376-79_1376-78insT
NM_002055.5:c.1172-79_1172-78insT MANE Select	NP_002046.1:n.1172-79_1172-78insT
NM_001242376.2:c.*2241_*2242insT	NP_001229305.1:n.*2241_*2242insT
NM_001363846.2:c.1292-79_1292-78insT	NP_001350775.1:n.1292-79_1292-78insT