Canonical Allele Identifier: CA399839231

Gene: GFAP

Linked Data

• MyVariant Identifiers: chr17:g.42985518C>A (hg19) ; chr17:g.44908150C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44908150C>A , CM000679.2:g.44908150C>A	GRCh38
NC_000017.10:g.42985518C>A , CM000679.1:g.42985518C>A	GRCh37
NC_000017.9:g.40341044C>A	NCBI36
NG_008401.1:g.12397G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000253408.11:c.1292-1G>T	ENSP00000253408.5:n.1292-1G>T
ENST00000253408.10:c.1292-1G>T	ENSP00000253408.5:n.1292-1G>T
ENST00000441312.2:n.25-1G>T
ENST00000585543.6:n.325-1G>T
ENST00000586125.2:c.107-1G>T	ENSP00000467397.2:n.107-1G>T
ENST00000588735.3:c.1172-1G>T MANE Select	ENSP00000466598.2:n.1172-1G>T
ENST00000589701.2:n.2078G>T
ENST00000591880.2:c.271-1G>T
ENST00000592065.2:n.539G>T
ENST00000638304.1:c.91-1G>T
ENST00000638400.1:c.7-1G>T
ENST00000638488.1:n.636-1G>T
ENST00000638618.1:c.827-1G>T	ENSP00000492832.1:n.827-1G>T
ENST00000638921.1:n.98G>T
ENST00000639042.1:c.144-1G>T
ENST00000639277.1:c.1172-1G>T	ENSP00000492432.1:n.1172-1G>T
ENST00000639369.1:c.22-1G>T
ENST00000253408.9:c.1172-1G>T	ENSP00000253408.4:n.1172-1G>T
ENST00000585543.5:n.325-1G>T
ENST00000586125.1:c.143-1G>T	ENSP00000467397.1:n.143-1G>T
ENST00000588640.5:n.552-1G>T
ENST00000588735.1:c.83-34G>T	ENSP00000466598.1:n.83-34G>T
ENST00000589701.1:n.73G>T
ENST00000591880.1:c.38-1G>T	ENSP00000467530.1:n.38-1G>T
ENST00000592706.5:n.44-1G>T
NM_002055.4:c.1172-1G>T	NP_002046.1:n.1172-1G>T
NM_001363846.1:c.1292-1G>T	NP_001350775.1:n.1292-1G>T
XM_024450690.1:c.1496-1G>T	XP_024306458.1:n.1496-1G>T
XM_024450692.1:c.1376-1G>T	XP_024306460.1:n.1376-1G>T
NM_002055.5:c.1172-1G>T MANE Select	NP_002046.1:n.1172-1G>T
NM_001363846.2:c.1292-1G>T	NP_001350775.1:n.1292-1G>T